annotate test-data/phenotypes-for-disease.tsv @ 1:7ae426ca9054 draft

planemo upload commit b538202f822ef9ce7af7f1ff2867dd1455b83725

DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002019	Constipation	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:12814332|PMID:21560061|PMID:23408927|PMID:22021174|PMID:19717168	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:614251	Parkinson Disease 18, Autosomal Dominant, Susceptibility to	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:614203	Parkinson Disease 17	RO:0002200	has phenotype	HP:0100660	Dyskinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0002015	Dysphagia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:614251	Parkinson Disease 18, Autosomal Dominant, Susceptibility to	RO:0002200	has phenotype	HP:0002322	Resting tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605543	Parkinson Disease 4, Autosomal Dominant	RO:0002200	has phenotype	HP:0001824	Weight loss	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606324	Parkinson Disease 7, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0000739	Anxiety	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168100	Paralysis Agitans, Juvenile, of Hunt	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:600116	Parkinson Disease 2, Autosomal Recessive Juvenile	RO:0002200	has phenotype	HP:0001332	Dystonia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0002020	Gastroesophageal reflux	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:614251	Parkinson Disease 18, Autosomal Dominant, Susceptibility to	RO:0002200	has phenotype	HP:0100315	Lewy bodies	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0000011	Neurogenic bladder	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:22331071|PMID:12922929|PMID:12756142|PMID:1965204|PMID:16855424	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0001824	Weight loss	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:20028343|PMID:16773618|PMID:15595933|PMID:11241387|PMID:21192784	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0000605	Supranuclear gaze palsy	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168601	autosomal dominant Parkinson disease 1	RO:0002200	has phenotype	HP:0000012	Urinary urgency	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0001621	Weak voice	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0100315	Lewy bodies	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605543	Parkinson Disease 4, Autosomal Dominant	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:22204976|PMID:23803637|PMID:16093408|PMID:23803638|PMID:16720791	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0001266	Choreoathetosis	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:2330103|PMID:1052297|PMID:6457534|PMID:16364674|PMID:9686783	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0000711	Restlessness	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:20683503|PMID:21560064|PMID:2350935|PMID:12390050|PMID:23047004	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615530	Parkinson Disease 20, Early-Onset	RO:0002200	has phenotype	HP:0001268	Mental deterioration	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168601	autosomal dominant Parkinson disease 1	RO:0002200	has phenotype	HP:0001260	Dysarthria	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:607060	autosomal dominant Parkinson disease 8	RO:0002200	has phenotype	HP:0002322	Resting tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615530	Parkinson Disease 20, Early-Onset	RO:0002200	has phenotype	HP:0002172	Postural instability	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605543	Parkinson Disease 4, Autosomal Dominant	RO:0002200	has phenotype	HP:0000726	Dementia	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605909	Parkinson Disease 6, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0002322	Resting tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0003881	Humeral sclerosis	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:21309754|PMID:10675426|PMID:9113500|PMID:22023479|PMID:19479510	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002076	Migraine	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:22037955|PMID:16870487|PMID:3431838|PMID:15090934|PMID:16341290	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260300	autosomal recessive early-onset Parkinson disease 15	RO:0002200	has phenotype	HP:0001337	Tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0100022	Abnormality of movement	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:21696993|PMID:22245219|PMID:17516489|PMID:17013911|PMID:17013922	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615530	Parkinson Disease 20, Early-Onset	RO:0002200	has phenotype	HP:0000658	Eyelid apraxia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0011968	Feeding difficulties	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615530	Parkinson Disease 20, Early-Onset	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260300	autosomal recessive early-onset Parkinson disease 15	RO:0002200	has phenotype	HP:0001332	Dystonia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260540	Parkinson-Dementia Syndrome	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0000975	Hyperhidrosis	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:22021174|PMID:7818245|PMID:20022689|PMID:14673882|PMID:15834763	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605909	Parkinson Disease 6, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0002172	Postural instability	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615528	Parkinson Disease 19, Juvenile-Onset	RO:0002200	has phenotype	HP:0000571	Hypometric saccades	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615530	Parkinson Disease 20, Early-Onset	RO:0002200	has phenotype	HP:0002362	Shuffling gait	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0000726	Dementia	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:14558483|PMID:11041086|PMID:22043625|PMID:23803637|PMID:11949709	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606324	Parkinson Disease 7, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0002322	Resting tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605909	Parkinson Disease 6, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:616361	Parkinson Disease 21	RO:0002200	has phenotype	HP:0100315	Lewy bodies	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0002172	Postural instability	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002511	Alzheimer disease	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:9843162|PMID:7652084|PMID:19367511|PMID:17514358|PMID:1311375	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:616361	Parkinson Disease 21	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615528	Parkinson Disease 19, Juvenile-Onset	RO:0002200	has phenotype	HP:0001260	Dysarthria	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:614203	Parkinson Disease 17	RO:0002200	has phenotype	HP:0002322	Resting tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002367	Visual hallucinations	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:16720791|PMID:7652084|PMID:20933338|PMID:16239760|PMID:17516497	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:600116	Parkinson Disease 2, Autosomal Recessive Juvenile	RO:0002200	has phenotype	HP:0002172	Postural instability	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0002019	Constipation	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168601	autosomal dominant Parkinson disease 1	RO:0002200	has phenotype	HP:0002322	Resting tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0003470	Paralysis	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:15728291|PMID:12654954|PMID:22130148|PMID:21560060|PMID:6231489	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:610297	Parkinson Disease 13, Autosomal Dominant, Susceptibility to	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:105500	Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1	RO:0002200	has phenotype	HP:0002366	Abnormal lower motor neuron morphology	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615530	Parkinson Disease 20, Early-Onset	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:14558491|PMID:15767513|PMID:17048150|PMID:8158173|PMID:20055267	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002359	Frequent falls	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:20411272|PMID:10191839|PMID:21764079|PMID:22776044|PMID:18608364	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:614203	Parkinson Disease 17	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002304	Akinesia	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:21840512|PMID:2515716|PMID:3730813|PMID:21560065|PMID:9549521	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:607060	autosomal dominant Parkinson disease 8	RO:0002200	has phenotype	HP:0002172	Postural instability	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168601	autosomal dominant Parkinson disease 1	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000501|ECO:0000501	evidence used in automatic assertion|evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605909	Parkinson Disease 6, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0000716	Depression	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615528	Parkinson Disease 19, Juvenile-Onset	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168601	autosomal dominant Parkinson disease 1	RO:0002200	has phenotype	HP:0001336	Myoclonus	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0001347	Hyperreflexia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:607060	autosomal dominant Parkinson disease 8	RO:0002200	has phenotype	HP:0011960	Substantia nigra gliosis	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0001337	Tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:607060	autosomal dominant Parkinson disease 8	RO:0002200	has phenotype	HP:0000726	Dementia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605543	Parkinson Disease 4, Autosomal Dominant	RO:0002200	has phenotype	HP:0011999	Paranoia	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:105500	Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1	RO:0002200	has phenotype	HP:0003394	Muscle cramps	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0003236	Elevated serum creatine phosphokinase	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0007311	Short stepped shuffling gait	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0100754	Mania	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:3167408|PMID:15291663|PMID:20205149|PMID:12034798|PMID:12465087	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0002304	Akinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:607060	autosomal dominant Parkinson disease 8	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002307	Drooling	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:11340798|PMID:2130649|PMID:11340797|PMID:17892967|PMID:22021174	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:607688	Parkinson Disease 11, Autosomal Dominant, Susceptibility to	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000269	experimental evidence used in manual assertion	PMID:18358451	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:600116	Parkinson Disease 2, Autosomal Recessive Juvenile	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0000605	Supranuclear gaze palsy	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:616361	Parkinson Disease 21	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0001257	Spasticity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0002062	Morphological abnormality of the pyramidal tract	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0100660	Dyskinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0007024	Pseudobulbar paralysis	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:3828155|PMID:8648326|PMID:3366147|PMID:8780066|PMID:12201229	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260540	Parkinson-Dementia Syndrome	RO:0002200	has phenotype	HP:0002493	Upper motor neuron dysfunction	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605909	Parkinson Disease 6, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0001332	Dystonia	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606324	Parkinson Disease 7, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002356	Writer's cramp	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:17131231|PMID:3504239|PMID:19232169|PMID:2296384|PMID:9074398	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0003006	Neuroblastoma	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:20026175|PMID:8341291|PMID:10737593|PMID:12787066|PMID:18411255	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0000298	Mask-like facies	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:600116	Parkinson Disease 2, Autosomal Recessive Juvenile	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002018	Nausea	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:17516484|PMID:21843110|PMID:19768728|PMID:2515717|PMID:6180142	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0000716	Depression	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0001347	Hyperreflexia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0001336	Myoclonus	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:18686651|PMID:1965204|PMID:2067442|PMID:12465085|PMID:2350935	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0000718	Aggressive behavior	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0001249	Intellectual disability	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:17548778|PMID:21257332|PMID:8665730|PMID:1618013|PMID:12836419	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605909	Parkinson Disease 6, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0001347	Hyperreflexia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:607060	autosomal dominant Parkinson disease 8	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615528	Parkinson Disease 19, Juvenile-Onset	RO:0002200	has phenotype	HP:0001337	Tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0001000	Abnormality of skin pigmentation	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:6499297|PMID:7715783|PMID:7771778|PMID:10737635|PMID:8731382	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0001263	Global developmental delay	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0003487	Babinski sign	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260300	autosomal recessive early-onset Parkinson disease 15	RO:0002200	has phenotype	HP:0002061	Lower limb spasticity	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260540	Parkinson-Dementia Syndrome	RO:0002200	has phenotype	HP:0001337	Tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168100	Paralysis Agitans, Juvenile, of Hunt	RO:0002200	has phenotype	HP:0001260	Dysarthria	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002529	Neuronal loss in central nervous system	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:23380027|PMID:17516497|PMID:18715146|PMID:22899187|PMID:17931705	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0000738	Hallucinations	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0001257	Spasticity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:600116	Parkinson Disease 2, Autosomal Recessive Juvenile	RO:0002200	has phenotype	HP:0001347	Hyperreflexia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0001260	Dysarthria	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0000012	Urinary urgency	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168601	autosomal dominant Parkinson disease 1	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:610297	Parkinson Disease 13, Autosomal Dominant, Susceptibility to	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0001268	Mental deterioration	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615528	Parkinson Disease 19, Juvenile-Onset	RO:0002200	has phenotype	HP:0002362	Shuffling gait	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0008936	Muscular hypotonia of the trunk	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0002172	Postural instability	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0002019	Constipation	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0001250	Seizures	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:616361	Parkinson Disease 21	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605543	Parkinson Disease 4, Autosomal Dominant	RO:0002200	has phenotype	HP:0001278	Orthostatic hypotension	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615528	Parkinson Disease 19, Juvenile-Onset	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0000751	Personality changes	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:600116	Parkinson Disease 2, Autosomal Recessive Juvenile	RO:0002200	has phenotype	HP:0001337	Tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615528	Parkinson Disease 19, Juvenile-Onset	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002331	Headache (with pheochromocytoma)	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:20464588|PMID:1807237|PMID:326325|PMID:11195537|PMID:17370756	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606324	Parkinson Disease 7, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0000643	Blepharospasm	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0002360	Sleep disturbance	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0011960	Substantia nigra gliosis	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260300	autosomal recessive early-onset Parkinson disease 15	RO:0002200	has phenotype	HP:0002548	Parkinsonism with favorable response to dopaminergic medication	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168601	autosomal dominant Parkinson disease 1	RO:0002200	has phenotype	HP:0002362	Shuffling gait	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615530	Parkinson Disease 20, Early-Onset	RO:0002200	has phenotype	HP:0001332	Dystonia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615528	Parkinson Disease 19, Juvenile-Onset	RO:0002200	has phenotype	HP:0001249	Intellectual disability	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0001332	Dystonia	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:614203	Parkinson Disease 17	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606324	Parkinson Disease 7, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0000725	Psychotic episodes	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260540	Parkinson-Dementia Syndrome	RO:0002200	has phenotype	HP:0000726	Dementia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605909	Parkinson Disease 6, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0000012	Urinary urgency	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605543	Parkinson Disease 4, Autosomal Dominant	RO:0002200	has phenotype	HP:0000738	Hallucinations	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002174	Postural tremor	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:19067999|PMID:20055267|PMID:18456512|PMID:19242649|PMID:17048150	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0000751	Personality changes	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168100	Paralysis Agitans, Juvenile, of Hunt	RO:0002200	has phenotype	HP:0001288	Gait disturbance	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:610297	Parkinson Disease 13, Autosomal Dominant, Susceptibility to	RO:0002200	has phenotype	HP:0002548	Parkinsonism with favorable response to dopaminergic medication	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:105500	Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:607060	autosomal dominant Parkinson disease 8	RO:0002200	has phenotype	HP:0002548	Parkinsonism with favorable response to dopaminergic medication	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0001337	Tremor	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:14558490|PMID:22976499|PMID:23047004|PMID:11949716|PMID:17516492	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168100	Paralysis Agitans, Juvenile, of Hunt	RO:0002200	has phenotype	HP:0001939	Abnormality of metabolism/homeostasis	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:607688	Parkinson Disease 11, Autosomal Dominant, Susceptibility to	RO:0002200	has phenotype	HP:0002172	Postural instability	ECO:0000269	experimental evidence used in manual assertion	PMID:18358451	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168601	autosomal dominant Parkinson disease 1	RO:0002200	has phenotype	HP:0002172	Postural instability	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260300	autosomal recessive early-onset Parkinson disease 15	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260540	Parkinson-Dementia Syndrome	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0002194	Delayed gross motor development	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260300	autosomal recessive early-onset Parkinson disease 15	RO:0002200	has phenotype	HP:0001347	Hyperreflexia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0000726	Dementia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0100753	Schizophrenia	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:10447302|PMID:19396395|PMID:8789910|PMID:17027767|PMID:9171838	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605909	Parkinson Disease 6, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002353	EEG abnormality	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:1714807|PMID:16483454|PMID:2605826|PMID:1753458|PMID:7489659	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260540	Parkinson-Dementia Syndrome	RO:0002200	has phenotype	HP:0002751	Kyphoscoliosis	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0000020	Urinary incontinence	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:12814332|PMID:15895303|PMID:19135266|PMID:22331072|PMID:20429324	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615528	Parkinson Disease 19, Juvenile-Onset	RO:0002200	has phenotype	HP:0001332	Dystonia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0000733	Stereotypic behavior	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:21072531|PMID:563012|PMID:16934409|PMID:3670611|PMID:6138131	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0100660	Dyskinesia	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:17013916|PMID:7146724|PMID:22043624|PMID:17516484|PMID:21729402	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0011951	Aspiration pneumonia	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:21098406|PMID:12970031|PMID:12404752|PMID:20518603|PMID:20869620	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0004409	Hyposmia	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:17508142|PMID:22035024|PMID:18322371|PMID:21560061|PMID:21387694	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615530	Parkinson Disease 20, Early-Onset	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0002548	Parkinsonism with favorable response to dopaminergic medication	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002167	Neurological speech impairment	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:19864662|PMID:8162135|PMID:15767513|PMID:22772465|PMID:22706836	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0002283	Global brain atrophy	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0002072	Chorea	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168100	Paralysis Agitans, Juvenile, of Hunt	RO:0002200	has phenotype	HP:0000298	Mask-like facies	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615530	Parkinson Disease 20, Early-Onset	RO:0002200	has phenotype	HP:0001260	Dysarthria	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002615	Hypotension	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:7296422|PMID:6441537|PMID:1300258|PMID:6180142|PMID:1300256	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0002172	Postural instability	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002172	Postural instability	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:20055267|PMID:12948464|PMID:3747258|PMID:17048150|PMID:22130147	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260300	autosomal recessive early-onset Parkinson disease 15	RO:0002200	has phenotype	HP:0002071	Abnormality of extrapyramidal motor function	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615530	Parkinson Disease 20, Early-Onset	RO:0002200	has phenotype	HP:0000605	Supranuclear gaze palsy	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0000726	Dementia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168601	autosomal dominant Parkinson disease 1	RO:0002200	has phenotype	HP:0002360	Sleep disturbance	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0100315	Lewy bodies	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:22043625|PMID:22245218|PMID:20055267|PMID:16093408|PMID:17516497	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0000738	Hallucinations	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:607688	Parkinson Disease 11, Autosomal Dominant, Susceptibility to	RO:0002200	has phenotype	HP:0002548	Parkinsonism with favorable response to dopaminergic medication	ECO:0000269	experimental evidence used in manual assertion	PMID:18358451	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:105500	Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1	RO:0002200	has phenotype	HP:0000726	Dementia	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260300	autosomal recessive early-onset Parkinson disease 15	RO:0002200	has phenotype	HP:0002172	Postural instability	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0001278	Orthostatic hypotension	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:21560061|PMID:16906622|PMID:12654979|PMID:12814332|PMID:5386267	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0000725	Psychotic episodes	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260300	autosomal recessive early-onset Parkinson disease 15	RO:0002200	has phenotype	HP:0000514	Slow saccadic eye movements	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168601	autosomal dominant Parkinson disease 1	RO:0002200	has phenotype	HP:0001332	Dystonia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:600116	Parkinson Disease 2, Autosomal Recessive Juvenile	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002322	Resting tremor	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:20055267|PMID:9426865|PMID:19176228|PMID:19858460|PMID:17048150	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:610297	Parkinson Disease 13, Autosomal Dominant, Susceptibility to	RO:0002200	has phenotype	HP:0001337	Tremor	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0001260	Dysarthria	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0000718	Aggressive behavior	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605909	Parkinson Disease 6, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0002312	Clumsiness	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0004409	Hyposmia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0000458	Anosmia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0100543	Cognitive impairment	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:18178571|PMID:17516457|PMID:9387801|PMID:18682443|PMID:20832408	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168601	autosomal dominant Parkinson disease 1	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0000738	Hallucinations	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:22043626|PMID:19507125|PMID:12814332|PMID:19680598|PMID:17548778	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260300	autosomal recessive early-onset Parkinson disease 15	RO:0002200	has phenotype	HP:0001260	Dysarthria	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0001336	Myoclonus	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168100	Paralysis Agitans, Juvenile, of Hunt	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:607060	autosomal dominant Parkinson disease 8	RO:0002200	has phenotype	HP:0004409	Hyposmia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260300	autosomal recessive early-onset Parkinson disease 15	RO:0002200	has phenotype	HP:0003487	Babinski sign	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606324	Parkinson Disease 7, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0006892	Frontotemporal cerebral atrophy	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0002936	Distal sensory impairment	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0000473	Torticollis	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260300	autosomal recessive early-onset Parkinson disease 15	RO:0002200	has phenotype	HP:0001762	Talipes equinovarus	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0002425	Anarthria	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:614203	Parkinson Disease 17	RO:0002200	has phenotype	HP:0002304	Akinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0001257	Spasticity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605909	Parkinson Disease 6, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0000726	Dementia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0000298	Mask-like facies	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:105500	Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1	RO:0002200	has phenotype	HP:0001324	Muscle weakness	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605543	Parkinson Disease 4, Autosomal Dominant	RO:0002200	has phenotype	HP:0002459	Dysautonomia	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260540	Parkinson-Dementia Syndrome	RO:0002200	has phenotype	HP:0002062	Morphological abnormality of the pyramidal tract	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260300	autosomal recessive early-onset Parkinson disease 15	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:614251	Parkinson Disease 18, Autosomal Dominant, Susceptibility to	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0002529	Neuronal loss in central nervous system	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0100595	Camptocormia	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:17027115|PMID:19864661|PMID:21389682|PMID:12671947|PMID:23994926	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615528	Parkinson Disease 19, Juvenile-Onset	RO:0002200	has phenotype	HP:0001250	Seizures	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168100	Paralysis Agitans, Juvenile, of Hunt	RO:0002200	has phenotype	HP:0001337	Tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0002493	Upper motor neuron dysfunction	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0001332	Dystonia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0002322	Resting tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0002459	Dysautonomia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615528	Parkinson Disease 19, Juvenile-Onset	RO:0002200	has phenotype	HP:0002493	Upper motor neuron dysfunction	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168601	autosomal dominant Parkinson disease 1	RO:0002200	has phenotype	HP:0001268	Mental deterioration	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0000722	Obsessive-compulsive behavior	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:20205149|PMID:15639176|PMID:21764406|PMID:22604202|PMID:23318227	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002180	Neurodegeneration	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:20865164|PMID:23040108|PMID:23019375|PMID:17255333|PMID:16720791	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605909	Parkinson Disease 6, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0000739	Anxiety	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168600	Parkinson Disease, Late-Onset	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:616361	Parkinson Disease 21	RO:0002200	has phenotype	HP:0001337	Tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168601	autosomal dominant Parkinson disease 1	RO:0002200	has phenotype	HP:0002015	Dysphagia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:607688	Parkinson Disease 11, Autosomal Dominant, Susceptibility to	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000269	experimental evidence used in manual assertion	PMID:18358451	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0002385	Paraparesis	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260300	autosomal recessive early-onset Parkinson disease 15	RO:0002200	has phenotype	HP:0012407	Scissor gait	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0001324	Muscle weakness	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:8682529|PMID:17931671|PMID:15372591|PMID:18313370|PMID:7659761	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002017	Nausea and vomiting	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:15495119|PMID:7195483|PMID:10091630|PMID:6481422|PMID:9756144	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:260540	Parkinson-Dementia Syndrome	RO:0002200	has phenotype	HP:0000597	Ophthalmoparesis	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:612953	Parkinson Disease 14, Autosomal Recessive	RO:0002200	has phenotype	HP:0001337	Tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606324	Parkinson Disease 7, Autosomal Recessive Early-Onset	RO:0002200	has phenotype	HP:0002174	Postural tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615530	Parkinson Disease 20, Early-Onset	RO:0002200	has phenotype	HP:0001337	Tremor	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0000017	Nocturia	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:11741097|PMID:8369103|PMID:19404716|PMID:20205139|PMID:21264941	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:600116	Parkinson Disease 2, Autosomal Recessive Juvenile	RO:0002200	has phenotype	HP:0011960	Substantia nigra gliosis	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:105500	Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1	RO:0002200	has phenotype	HP:0007354	Amyotrophic lateral sclerosis	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002072	Chorea	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:1656540|PMID:1557069|PMID:21729402|PMID:9387799|PMID:39737	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0010524	Agnosia	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:2932922|PMID:12796834|PMID:15782604|PMID:9686278|PMID:3263977	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0000709	Psychosis	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:21630354|PMID:12814332|PMID:17013906|PMID:10727476|PMID:22245219	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:613135	Parkinsonism-Dystonia, Infantile	RO:0002200	has phenotype	HP:0002451	Limb dystonia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:22402215|PMID:11949716|PMID:9513304|PMID:20055267|PMID:17048150	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:168100	Paralysis Agitans, Juvenile, of Hunt	RO:0002200	has phenotype	HP:0002063	Rigidity	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0001332	Dystonia	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:2515718|PMID:6231489|PMID:22976499|PMID:2579626|PMID:7715793	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:614251	Parkinson Disease 18, Autosomal Dominant, Susceptibility to	RO:0002200	has phenotype	HP:0002067	Bradykinesia	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:606693	Kufor-Rakeb syndrome	RO:0002200	has phenotype	HP:0000514	Slow saccadic eye movements	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:614203	Parkinson Disease 17	RO:0002200	has phenotype	HP:0002172	Postural instability	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:614203	Parkinson Disease 17	RO:0002200	has phenotype	HP:0001300	Parkinsonism	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:615528	Parkinson Disease 19, Juvenile-Onset	RO:0002200	has phenotype	HP:0002172	Postural instability	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:105500	Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1	RO:0002200	has phenotype	HP:0001283	Bulbar palsy	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:600116	Parkinson Disease 2, Autosomal Recessive Juvenile	RO:0002200	has phenotype	HP:0001288	Gait disturbance	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0000751	Personality changes	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:21560061|PMID:16908734|PMID:21845593|PMID:9426865|PMID:18346925	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:616361	Parkinson Disease 21	RO:0002200	has phenotype	HP:0002172	Postural instability	ECO:0000501	evidence used in automatic assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0002321	Vertigo	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:19479494|PMID:21843110|PMID:19768728|PMID:2515717|PMID:12814332	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:607688	Parkinson Disease 11, Autosomal Dominant, Susceptibility to	RO:0002200	has phenotype	HP:0002322	Resting tremor	ECO:0000269	experimental evidence used in manual assertion	PMID:18358451	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0000746	Delusions	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:12814332|PMID:16239760|PMID:7652084|PMID:19507125|PMID:20538500	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0000822	Hypertension	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:18166127|PMID:20032288|PMID:11041086|PMID:17761552|PMID:17514358	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
OMIM:605543	Parkinson Disease 4, Autosomal Dominant	RO:0002200	has phenotype	HP:0100315	Lewy bodies	ECO:0000304	traceable author statement used in manual assertion		http://data.monarchinitiative.org/ttl/hpoa.ttl	direct
DOID:14330	Parkinson's disease	RO:0002200	has phenotype	HP:0000012	Urinary urgency	ECO:0000246	computational combinatorial evidence used in automatic assertion	PMID:3942028|PMID:14521485|PMID:18327532|PMID:19908315|PMID:11570707	http://data.monarchinitiative.org/ttl/hpoa.ttl	direct