Human Phenotype Ontology

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0000738	HP:0000738	Hallucinations	0	ABCA7 CL E G H	10347	37	ORPHA:1020	Early-onset autosomal dominant Alzheimer disease	HP:0040281 - Very frequent	3
HP:0000738	HP:0000738	Hallucinations	0	ADGRV1 CL E G H	84059	17416	ORPHA:231178	Usher syndrome type 2	HP:0040283 - Occasional	530
HP:0000738	HP:0000738	Hallucinations	0	ADH1C CL E G H	126	251	OMIM:168600	Parkinson disease, late-onset	HP:0040283 - Occasional	4
HP:0000738	HP:0000738	Hallucinations	0	ALAD CL E G H	210	395	ORPHA:100924	Porphyria due to ALA dehydratase deficiency	HP:0040283 - Occasional	62
HP:0000738	HP:0000738	Hallucinations	0	ALDH4A1 CL E G H	8659	406	ORPHA:79101	Hyperprolinemia type 2	HP:0040283 - Occasional	74
HP:0000738	HP:0000738	Hallucinations	0	ALDH5A1 CL E G H	7915	408	OMIM:271980	Succinic semialdehyde dehydrogenase deficiency	.	108
HP:0000738	HP:0000738	Hallucinations	0	APOL2 CL E G H	23780	619	OMIM:181500	SCHIZOPHRENIA	.
HP:0000738	HP:0000738	Hallucinations	0	APOL4 CL E G H	80832	14867	OMIM:181500	SCHIZOPHRENIA	.
HP:0000738	HP:0000738	Hallucinations	0	APP CL E G H	351	620	ORPHA:1020	Early-onset autosomal dominant Alzheimer disease	HP:0040281 - Very frequent	74
HP:0000738	HP:0000738	Hallucinations	0	ARSA CL E G H	410	713	OMIM:250100	Metachromatic leukodystrophy	.	253
HP:0000738	HP:0000738	Hallucinations	0	ARSA CL E G H	410	713	ORPHA:309271	Metachromatic leukodystrophy, adult form	HP:0040282 - Frequent	253
HP:0000738	HP:0000738	Hallucinations	0	ARSA CL E G H	410	713	ORPHA:309263	Metachromatic leukodystrophy, juvenile form	HP:0040283 - Occasional	253
HP:0000738	HP:0000738	Hallucinations	0	ARSA CL E G H	410	713	ORPHA:309256	Metachromatic leukodystrophy, late infantile form	HP:0040283 - Occasional	253
HP:0000738	HP:0000738	Hallucinations	0	ARSG CL E G H	22901	24102	ORPHA:231183	Usher syndrome type 3	HP:0040283 - Occasional
HP:0000738	HP:0000738	Hallucinations	0	ATP13A2 CL E G H	23400	30213	ORPHA:513436	Autosomal recessive spastic paraplegia type 78	HP:0040284 - Very rare	100
HP:0000738	HP:0000738	Hallucinations	0	ATP13A2 CL E G H	23400	30213	ORPHA:306674	Kufor-Rakeb syndrome		100
HP:0000738	HP:0000738	Hallucinations	0	ATP13A2 CL E G H	23400	30213	OMIM:606693	Kufor-Rakeb syndrome		100
HP:0000738	HP:0000738	Hallucinations	0	ATP13A2 CL E G H	23400	30213	OMIM:617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE; SPG78		100
HP:0000738	HP:0000738	Hallucinations	0	ATXN2 CL E G H	6311	10555	OMIM:168600	Parkinson disease, late-onset	HP:0040283 - Occasional	11
HP:0000738	HP:0000738	Hallucinations	0	ATXN8OS CL E G H	6315	10561	OMIM:168600	Parkinson disease, late-onset	HP:0040283 - Occasional	1
HP:0000738	HP:0000738	Hallucinations	0	BCKDHA CL E G H	593	986	OMIM:248600	Maple syrup urine disease	.	120
HP:0000738	HP:0000738	Hallucinations	0	BCKDHB CL E G H	594	987	OMIM:248600	Maple syrup urine disease	.	162
HP:0000738	HP:0000738	Hallucinations	0	BCS1L CL E G H	617	1020	OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1	.	72
HP:0000738	HP:0000738	Hallucinations	0	BMPR1A CL E G H	657	1076	ORPHA:440437	Familial colorectal cancer Type X	HP:0040283 - Occasional	385
HP:0000738	HP:0000738	Hallucinations	0	BPTF CL E G H	2186	3581	ORPHA:529962	17q24.2 microdeletion syndrome	HP:0040283 - Occasional	2
HP:0000738	HP:0000738	Hallucinations	0	C9ORF72 CL E G H	203228	28337	OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1	.	56
HP:0000738	HP:0000738	Hallucinations	0	C9ORF72 CL E G H	203228	28337	ORPHA:275872	Frontotemporal dementia with motor neuron disease	HP:0040282 - Frequent	56
HP:0000738	HP:0000738	Hallucinations	0	CACNA1A CL E G H	773	1388	OMIM:141500	Migraine, familial hemiplegic, 1		449
HP:0000738	HP:0000738	Hallucinations	0	CDH2 CL E G H	1000	1759	OMIM:618929	AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME; ACOGS
HP:0000738	HP:0000738	Hallucinations	0	CDH23 CL E G H	64072	13733	ORPHA:231169	Usher syndrome type 1	HP:0040283 - Occasional	636
HP:0000738	HP:0000738	Hallucinations	0	CEP78 CL E G H	84131	25740	ORPHA:231183	Usher syndrome type 3	HP:0040283 - Occasional	9
HP:0000738	HP:0000738	Hallucinations	0	CEP85L CL E G H	387119	21638	OMIM:618873	LISSENCEPHALY 10; LIS10		1
HP:0000738	HP:0000738	Hallucinations	0	CHCHD10 CL E G H	400916	15559	ORPHA:275872	Frontotemporal dementia with motor neuron disease	HP:0040282 - Frequent	11
HP:0000738	HP:0000738	Hallucinations	0	CHI3L1 CL E G H	1116	1932	OMIM:181500	SCHIZOPHRENIA	.	1
HP:0000738	HP:0000738	Hallucinations	0	CIB2 CL E G H	10518	24579	ORPHA:231169	Usher syndrome type 1	HP:0040283 - Occasional	15
HP:0000738	HP:0000738	Hallucinations	0	CISD2 CL E G H	493856	24212	ORPHA:3463	Wolfram syndrome	HP:0040283 - Occasional	3
HP:0000738	HP:0000738	Hallucinations	0	CLN3 CL E G H	1201	2074	ORPHA:228346	CLN3 disease		216
HP:0000738	HP:0000738	Hallucinations	0	CLN5 CL E G H	1203	2076	ORPHA:228360	CLN5 disease	HP:0040283 - Occasional	141
HP:0000738	HP:0000738	Hallucinations	0	CLN6 CL E G H	54982	2077	OMIM:204300	Ceroid lipofuscinosis, neuronal, 4A, autosomal recessive		143
HP:0000738	HP:0000738	Hallucinations	0	CLRN1 CL E G H	7401	12605	ORPHA:231183	Usher syndrome type 3	HP:0040283 - Occasional	60
HP:0000738	HP:0000738	Hallucinations	0	CLTRN CL E G H	57393	29437	ORPHA:2116	Hartnup disease	HP:0040281 - Very frequent
HP:0000738	HP:0000738	Hallucinations	0	COMT CL E G H	1312	2228	OMIM:181500	SCHIZOPHRENIA	.	6
HP:0000738	HP:0000738	Hallucinations	0	CPOX CL E G H	1371	2321	OMIM:121300	Coproporphyria	.	72
HP:0000738	HP:0000738	Hallucinations	0	CSF1R CL E G H	1436	2433	OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		149
HP:0000738	HP:0000738	Hallucinations	0	CTSH CL E G H	1512	2535	ORPHA:2073	Narcolepsy type 1	HP:0040281 - Very frequent	1
HP:0000738	HP:0000738	Hallucinations	0	CYP27A1 CL E G H	1593	2605	OMIM:213700	Cerebrotendinous xanthomatosis	.	114
HP:0000738	HP:0000738	Hallucinations	0	CYP27A1 CL E G H	1593	2605	ORPHA:909	Cerebrotendinous xanthomatosis	HP:0040283 - Occasional	114
HP:0000738	HP:0000738	Hallucinations	0	DAOA CL E G H	267012	21191	OMIM:181500	SCHIZOPHRENIA	.
HP:0000738	HP:0000738	Hallucinations	0	DBT CL E G H	1629	2698	OMIM:248600	Maple syrup urine disease	.	156
HP:0000738	HP:0000738	Hallucinations	0	DCAF17 CL E G H	80067	25784	ORPHA:3464	Woodhouse-Sakati syndrome	HP:0040283 - Occasional	87
HP:0000738	HP:0000738	Hallucinations	0	DCAF17 CL E G H	80067	25784	OMIM:241080	Woodhouse-Sakati syndrome	HP:0040283 - Occasional	87
HP:0000738	HP:0000738	Hallucinations	0	DEPDC5 CL E G H	9681	18423	ORPHA:101046	Autosomal dominant epilepsy with auditory features		172
HP:0000738	HP:0000738	Hallucinations	0	DEPDC5 CL E G H	9681	18423	ORPHA:98820	Familial focal epilepsy with variable foci		172
HP:0000738	HP:0000738	Hallucinations	0	DISC2 CL E G H	27184	2889	OMIM:181500	SCHIZOPHRENIA	.
HP:0000738	HP:0000738	Hallucinations	0	DNAJC13 CL E G H	23317	30343	ORPHA:411602	Hereditary late-onset Parkinson disease		2
HP:0000738	HP:0000738	Hallucinations	0	DNAJC5 CL E G H	80331	16235	OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		155
HP:0000738	HP:0000738	Hallucinations	0	DNAJC6 CL E G H	9829	15469	OMIM:615528	Parkinson disease 19a, juvenile-onset	.	6
HP:0000738	HP:0000738	Hallucinations	0	DNAJC6 CL E G H	9829	15469	ORPHA:2828	Young-onset Parkinson disease	HP:0040282 - Frequent	6
HP:0000738	HP:0000738	Hallucinations	0	DNM1L CL E G H	10059	2973	ORPHA:98673	Autosomal dominant optic atrophy, classic form	HP:0040284 - Very rare	94
HP:0000738	HP:0000738	Hallucinations	0	DRD3 CL E G H	1814	3024	OMIM:181500	SCHIZOPHRENIA	.	21
HP:0000738	HP:0000738	Hallucinations	0	ECM1 CL E G H	1893	3153	OMIM:247100	Urbach-Wiethe disease	.	14
HP:0000738	HP:0000738	Hallucinations	0	EIF4G1 CL E G H	1981	3296	ORPHA:411602	Hereditary late-onset Parkinson disease		2
HP:0000738	HP:0000738	Hallucinations	0	EPCAM CL E G H	4072	11529	ORPHA:144	Lynch syndrome	HP:0040283 - Occasional	170
HP:0000738	HP:0000738	Hallucinations	0	EPM2A CL E G H	7957	3413	ORPHA:501	Lafora disease		83
HP:0000738	HP:0000738	Hallucinations	0	EPM2A CL E G H	7957	3413	OMIM:254780	Myoclonic epilepsy of lafora		83
HP:0000738	HP:0000738	Hallucinations	0	ESPN CL E G H	83715	13281	ORPHA:231169	Usher syndrome type 1	HP:0040283 - Occasional	33
HP:0000738	HP:0000738	Hallucinations	0	FAN1 CL E G H	22909	29170	ORPHA:144	Lynch syndrome	HP:0040283 - Occasional	15
HP:0000738	HP:0000738	Hallucinations	0	FBXO7 CL E G H	25793	13586	ORPHA:171695	Parkinsonian-pyramidal syndrome		36
HP:0000738	HP:0000738	Hallucinations	0	FIG4 CL E G H	9896	16873	ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		111
HP:0000738	HP:0000738	Hallucinations	0	FIG4 CL E G H	9896	16873	OMIM:612691	Polymicrogyria, bilateral temporooccipital		111
HP:0000738	HP:0000738	Hallucinations	0	FUS CL E G H	2521	4010	ORPHA:275872	Frontotemporal dementia with motor neuron disease	HP:0040282 - Frequent	105
HP:0000738	HP:0000738	Hallucinations	0	GBA1 CL E G H	2629	4177	OMIM:127750	Dementia, lewy body
HP:0000738	HP:0000738	Hallucinations	0	GBA1 CL E G H	2629	4177	ORPHA:411602	Hereditary late-onset Parkinson disease
HP:0000738	HP:0000738	Hallucinations	0	GBA1 CL E G H	2629	4177	OMIM:168600	Parkinson disease, late-onset	HP:0040283 - Occasional
HP:0000738	HP:0000738	Hallucinations	0	GIGYF2 CL E G H	26058	11960	ORPHA:411602	Hereditary late-onset Parkinson disease		8
HP:0000738	HP:0000738	Hallucinations	0	GLUD2 CL E G H	2747	4336	OMIM:168600	Parkinson disease, late-onset	HP:0040283 - Occasional	1
HP:0000738	HP:0000738	Hallucinations	0	GRN CL E G H	2896	4601	OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions	.	126
HP:0000738	HP:0000738	Hallucinations	0	HARS1 CL E G H	3035	4816	ORPHA:231183	Usher syndrome type 3	HP:0040283 - Occasional
HP:0000738	HP:0000738	Hallucinations	0	HCRT CL E G H	3060	4847	OMIM:161400	Narcolepsy 1		1
HP:0000738	HP:0000738	Hallucinations	0	HCRT CL E G H	3060	4847	ORPHA:2073	Narcolepsy type 1	HP:0040281 - Very frequent	1
HP:0000738	HP:0000738	Hallucinations	0	HCRT CL E G H	3060	4847	ORPHA:83465	Narcolepsy type 2	HP:0040281 - Very frequent	1
HP:0000738	HP:0000738	Hallucinations	0	HLA-DQB1 CL E G H	3119	4944	OMIM:123400	Creutzfeldt-Jakob disease	.
HP:0000738	HP:0000738	Hallucinations	0	HLA-DQB1 CL E G H	3119	4944	ORPHA:2073	Narcolepsy type 1	HP:0040281 - Very frequent
HP:0000738	HP:0000738	Hallucinations	0	HLA-DQB1 CL E G H	3119	4944	ORPHA:83465	Narcolepsy type 2	HP:0040281 - Very frequent
HP:0000738	HP:0000738	Hallucinations	0	HLA-DRB1 CL E G H	3123	4948	ORPHA:2073	Narcolepsy type 1	HP:0040281 - Very frequent	2
HP:0000738	HP:0000738	Hallucinations	0	HLA-DRB1 CL E G H	3123	4948	ORPHA:83465	Narcolepsy type 2	HP:0040281 - Very frequent	2
HP:0000738	HP:0000738	Hallucinations	0	HMBS CL E G H	3145	4982	ORPHA:79276	Acute intermittent porphyria	HP:0040283 - Occasional	81
HP:0000738	HP:0000738	Hallucinations	0	HTR2A CL E G H	3356	5293	OMIM:181500	SCHIZOPHRENIA	.	4
HP:0000738	HP:0000738	Hallucinations	0	HTRA1 CL E G H	5654	9476	OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		34
HP:0000738	HP:0000738	Hallucinations	0	HTRA2 CL E G H	27429	14348	ORPHA:2828	Young-onset Parkinson disease	HP:0040282 - Frequent	39
HP:0000738	HP:0000738	Hallucinations	0	HTT CL E G H	3064	4851	ORPHA:399	Huntington disease	HP:0040282 - Frequent	12
HP:0000738	HP:0000738	Hallucinations	0	JPH3 CL E G H	57338	14203	OMIM:606438	Huntington disease-like 2	.	2
HP:0000738	HP:0000738	Hallucinations	0	KRAS CL E G H	3845	6407	ORPHA:144	Lynch syndrome	HP:0040283 - Occasional	196
HP:0000738	HP:0000738	Hallucinations	0	LGI1 CL E G H	9211	6572	ORPHA:101046	Autosomal dominant epilepsy with auditory features		75
HP:0000738	HP:0000738	Hallucinations	0	LRRK2 CL E G H	120892	18618	ORPHA:411602	Hereditary late-onset Parkinson disease		221
HP:0000738	HP:0000738	Hallucinations	0	LRRK2 CL E G H	120892	18618	ORPHA:2828	Young-onset Parkinson disease	HP:0040282 - Frequent	221
HP:0000738	HP:0000738	Hallucinations	0	MAN2B1 CL E G H	4125	6826	ORPHA:309288	Alpha-mannosidosis, adult form	HP:0040283 - Occasional	136
HP:0000738	HP:0000738	Hallucinations	0	MAN2B1 CL E G H	4125	6826	ORPHA:309282	Alpha-mannosidosis, infantile form	HP:0040283 - Occasional	136
HP:0000738	HP:0000738	Hallucinations	0	MAPT CL E G H	4137	6893	OMIM:168600	Parkinson disease, late-onset	HP:0040283 - Occasional	140
HP:0000738	HP:0000738	Hallucinations	0	MED12 CL E G H	9968	11957	ORPHA:776	Lujan-Fryns syndrome	HP:0040283 - Occasional	228
HP:0000738	HP:0000738	Hallucinations	0	MLH1 CL E G H	4292	7127	ORPHA:144	Lynch syndrome	HP:0040283 - Occasional	1819
HP:0000738	HP:0000738	Hallucinations	0	MLH3 CL E G H	27030	7128	ORPHA:144	Lynch syndrome	HP:0040283 - Occasional	131
HP:0000738	HP:0000738	Hallucinations	0	MMACHC CL E G H	25974	24525	ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		101
HP:0000738	HP:0000738	Hallucinations	0	MOG CL E G H	4340	7197	ORPHA:2073	Narcolepsy type 1	HP:0040281 - Very frequent	1
HP:0000738	HP:0000738	Hallucinations	0	MSH2 CL E G H	4436	7325	ORPHA:144	Lynch syndrome	HP:0040283 - Occasional	2162
HP:0000738	HP:0000738	Hallucinations	0	MSH6 CL E G H	2956	7329	ORPHA:144	Lynch syndrome	HP:0040283 - Occasional	2232
HP:0000738	HP:0000738	Hallucinations	0	MTHFR CL E G H	4524	7436	OMIM:181500	SCHIZOPHRENIA	.	183
HP:0000738	HP:0000738	Hallucinations	0	MYO7A CL E G H	4647	7606	ORPHA:231169	Usher syndrome type 1	HP:0040283 - Occasional	516
HP:0000738	HP:0000738	Hallucinations	0	MYO7A CL E G H	4647	7606	ORPHA:231178	Usher syndrome type 2	HP:0040283 - Occasional	516
HP:0000738	HP:0000738	Hallucinations	0	NDP CL E G H	4693	7678	OMIM:310600	Norrie disease	.	39
HP:0000738	HP:0000738	Hallucinations	0	NDP CL E G H	4693	7678	ORPHA:649	Norrie disease	HP:0040283 - Occasional	39
HP:0000738	HP:0000738	Hallucinations	0	NHLRC1 CL E G H	378884	21576	ORPHA:501	Lafora disease		77
HP:0000738	HP:0000738	Hallucinations	0	NHLRC1 CL E G H	378884	21576	OMIM:254780	Myoclonic epilepsy of lafora		77
HP:0000738	HP:0000738	Hallucinations	0	NPRL2 CL E G H	10641	24969	ORPHA:98820	Familial focal epilepsy with variable foci		4
HP:0000738	HP:0000738	Hallucinations	0	NPRL3 CL E G H	8131	14124	ORPHA:98820	Familial focal epilepsy with variable foci		7
HP:0000738	HP:0000738	Hallucinations	0	NR4A2 CL E G H	4929	7981	OMIM:168600	Parkinson disease, late-onset	HP:0040283 - Occasional	27
HP:0000738	HP:0000738	Hallucinations	0	OPA1 CL E G H	4976	8140	ORPHA:98673	Autosomal dominant optic atrophy, classic form	HP:0040284 - Very rare	214
HP:0000738	HP:0000738	Hallucinations	0	P2RY11 CL E G H	5032	8540	ORPHA:2073	Narcolepsy type 1	HP:0040281 - Very frequent	2
HP:0000738	HP:0000738	Hallucinations	0	PARK7 CL E G H	11315	16369	ORPHA:2828	Young-onset Parkinson disease	HP:0040282 - Frequent	23
HP:0000738	HP:0000738	Hallucinations	0	PCDH15 CL E G H	65217	14674	ORPHA:231169	Usher syndrome type 1	HP:0040283 - Occasional	352
HP:0000738	HP:0000738	Hallucinations	0	PDZD7 CL E G H	79955	26257	ORPHA:231178	Usher syndrome type 2	HP:0040283 - Occasional	40
HP:0000738	HP:0000738	Hallucinations	0	PIK3CA CL E G H	5290	8975	ORPHA:144	Lynch syndrome	HP:0040283 - Occasional	162
HP:0000738	HP:0000738	Hallucinations	0	PINK1 CL E G H	65018	14581	ORPHA:2828	Young-onset Parkinson disease	HP:0040282 - Frequent	55
HP:0000738	HP:0000738	Hallucinations	0	PMS1 CL E G H	5378	9121	ORPHA:144	Lynch syndrome	HP:0040283 - Occasional	56
HP:0000738	HP:0000738	Hallucinations	0	PMS2 CL E G H	5395	9122	ORPHA:144	Lynch syndrome	HP:0040283 - Occasional	1121
HP:0000738	HP:0000738	Hallucinations	0	PODXL CL E G H	5420	9171	ORPHA:2828	Young-onset Parkinson disease	HP:0040282 - Frequent	6
HP:0000738	HP:0000738	Hallucinations	0	PPOX CL E G H	5498	9280	ORPHA:79473	Porphyria variegata	HP:0040284 - Very rare	41
HP:0000738	HP:0000738	Hallucinations	0	PPT1 CL E G H	5538	9325	OMIM:256730	Ceroid lipofuscinosis, neuronal, 1	.	172
HP:0000738	HP:0000738	Hallucinations	0	PRDM8 CL E G H	56978	13993	OMIM:616640	Epilepsy, progressive myoclonic, 10		1
HP:0000738	HP:0000738	Hallucinations	0	PRKN CL E G H	5071	8607	ORPHA:2828	Young-onset Parkinson disease	HP:0040282 - Frequent	138
HP:0000738	HP:0000738	Hallucinations	0	PRNP CL E G H	5621	9449	OMIM:123400	Creutzfeldt-Jakob disease	.	69
HP:0000738	HP:0000738	Hallucinations	0	PRNP CL E G H	5621	9449	ORPHA:282166	Inherited Creutzfeldt-Jakob disease	HP:0040283 - Occasional	69
HP:0000738	HP:0000738	Hallucinations	0	PSAP CL E G H	5660	9498	ORPHA:309271	Metachromatic leukodystrophy, adult form	HP:0040282 - Frequent	81
HP:0000738	HP:0000738	Hallucinations	0	PSAP CL E G H	5660	9498	ORPHA:309263	Metachromatic leukodystrophy, juvenile form	HP:0040283 - Occasional	81
HP:0000738	HP:0000738	Hallucinations	0	PSAP CL E G H	5660	9498	ORPHA:309256	Metachromatic leukodystrophy, late infantile form	HP:0040283 - Occasional	81
HP:0000738	HP:0000738	Hallucinations	0	PSEN1 CL E G H	5663	9508	ORPHA:1020	Early-onset autosomal dominant Alzheimer disease	HP:0040281 - Very frequent	241
HP:0000738	HP:0000738	Hallucinations	0	PSEN2 CL E G H	5664	9509	ORPHA:1020	Early-onset autosomal dominant Alzheimer disease	HP:0040281 - Very frequent	59
HP:0000738	HP:0000738	Hallucinations	0	PSMD12 CL E G H	5718	9557	ORPHA:529962	17q24.2 microdeletion syndrome	HP:0040283 - Occasional	4
HP:0000738	HP:0000738	Hallucinations	0	PUS3 CL E G H	83480	25461	ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		1
HP:0000738	HP:0000738	Hallucinations	0	RELN CL E G H	5649	9957	ORPHA:101046	Autosomal dominant epilepsy with auditory features		334
HP:0000738	HP:0000738	Hallucinations	0	RPS20 CL E G H	6224	10405	ORPHA:440437	Familial colorectal cancer Type X	HP:0040283 - Occasional	1
HP:0000738	HP:0000738	Hallucinations	0	RTN4R CL E G H	65078	18601	OMIM:181500	SCHIZOPHRENIA	.	2
HP:0000738	HP:0000738	Hallucinations	0	SEMA4A CL E G H	64218	10729	ORPHA:440437	Familial colorectal cancer Type X	HP:0040283 - Occasional	48
HP:0000738	HP:0000738	Hallucinations	0	SLC25A13 CL E G H	10165	10983	ORPHA:247585	Citrullinemia type II	HP:0040282 - Frequent	82
HP:0000738	HP:0000738	Hallucinations	0	SLC2A3 CL E G H	6515	11007	ORPHA:399	Huntington disease	HP:0040282 - Frequent	1
HP:0000738	HP:0000738	Hallucinations	0	SLC6A19 CL E G H	340024	27960	ORPHA:2116	Hartnup disease	HP:0040281 - Very frequent	12
HP:0000738	HP:0000738	Hallucinations	0	SNCA CL E G H	6622	11138	OMIM:127750	Dementia, lewy body		65
HP:0000738	HP:0000738	Hallucinations	0	SNCA CL E G H	6622	11138	ORPHA:411602	Hereditary late-onset Parkinson disease		65
HP:0000738	HP:0000738	Hallucinations	0	SNCA CL E G H	6622	11138	OMIM:168601	Parkinson disease 1, autosomal dominant	.	65
HP:0000738	HP:0000738	Hallucinations	0	SNCA CL E G H	6622	11138	OMIM:605543	Parkinson disease 4	.	65
HP:0000738	HP:0000738	Hallucinations	0	SNCA CL E G H	6622	11138	ORPHA:171695	Parkinsonian-pyramidal syndrome		65
HP:0000738	HP:0000738	Hallucinations	0	SNCA CL E G H	6622	11138	ORPHA:2828	Young-onset Parkinson disease	HP:0040282 - Frequent	65
HP:0000738	HP:0000738	Hallucinations	0	SNCAIP CL E G H	9627	11139	OMIM:168600	Parkinson disease, late-onset	HP:0040283 - Occasional	35
HP:0000738	HP:0000738	Hallucinations	0	SNCB CL E G H	6620	11140	OMIM:127750	Dementia, lewy body		2
HP:0000738	HP:0000738	Hallucinations	0	SON CL E G H	6651	11183	ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		12
HP:0000738	HP:0000738	Hallucinations	0	SORL1 CL E G H	6653	11185	ORPHA:1020	Early-onset autosomal dominant Alzheimer disease	HP:0040281 - Very frequent	3
HP:0000738	HP:0000738	Hallucinations	0	SPART CL E G H	23111	18514	ORPHA:101000	Autosomal recessive spastic paraplegia type 20	HP:0040283 - Occasional	66
HP:0000738	HP:0000738	Hallucinations	0	SQSTM1 CL E G H	8878	11280	ORPHA:275872	Frontotemporal dementia with motor neuron disease	HP:0040282 - Frequent	62
HP:0000738	HP:0000738	Hallucinations	0	SYN2 CL E G H	6854	11495	OMIM:181500	SCHIZOPHRENIA	.	3
HP:0000738	HP:0000738	Hallucinations	0	SYNJ1 CL E G H	8867	11503	ORPHA:2828	Young-onset Parkinson disease	HP:0040282 - Frequent	9
HP:0000738	HP:0000738	Hallucinations	0	TARDBP CL E G H	23435	11571	ORPHA:275872	Frontotemporal dementia with motor neuron disease	HP:0040282 - Frequent	65
HP:0000738	HP:0000738	Hallucinations	0	TBK1 CL E G H	29110	11584	ORPHA:275872	Frontotemporal dementia with motor neuron disease	HP:0040282 - Frequent	20
HP:0000738	HP:0000738	Hallucinations	0	TBP CL E G H	6908	11588	OMIM:168600	Parkinson disease, late-onset	HP:0040283 - Occasional	7
HP:0000738	HP:0000738	Hallucinations	0	TBP CL E G H	6908	11588	OMIM:607136	Spinocerebellar ataxia 17	.	7
HP:0000738	HP:0000738	Hallucinations	0	TGFBR2 CL E G H	7048	11773	ORPHA:144	Lynch syndrome	HP:0040283 - Occasional	253
HP:0000738	HP:0000738	Hallucinations	0	TNFSF4 CL E G H	7292	11934	ORPHA:2073	Narcolepsy type 1	HP:0040281 - Very frequent
HP:0000738	HP:0000738	Hallucinations	0	TOMM40 CL E G H	10452	18001	ORPHA:1020	Early-onset autosomal dominant Alzheimer disease	HP:0040281 - Very frequent
HP:0000738	HP:0000738	Hallucinations	0	TREM2 CL E G H	54209	17761	ORPHA:1020	Early-onset autosomal dominant Alzheimer disease	HP:0040281 - Very frequent	31
HP:0000738	HP:0000738	Hallucinations	0	TRNS2 CL E G H	4575	7498	ORPHA:231183	Usher syndrome type 3	HP:0040283 - Occasional
HP:0000738	HP:0000738	Hallucinations	0	TRNT CL E G H	4576	7499	OMIM:168600	Parkinson disease, late-onset	HP:0040283 - Occasional
HP:0000738	HP:0000738	Hallucinations	0	TRRAP CL E G H	8295	12347	OMIM:618454	Developmental delay with or without dysmorphic facies and autism		2
HP:0000738	HP:0000738	Hallucinations	0	TTC19 CL E G H	54902	26006	OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2	.	88
HP:0000738	HP:0000738	Hallucinations	0	UCHL1 CL E G H	7345	12513	ORPHA:2828	Young-onset Parkinson disease	HP:0040282 - Frequent	21
HP:0000738	HP:0000738	Hallucinations	0	UPF3B CL E G H	65109	20439	ORPHA:776	Lujan-Fryns syndrome	HP:0040283 - Occasional	33
HP:0000738	HP:0000738	Hallucinations	0	USH1C CL E G H	10083	12597	ORPHA:231169	Usher syndrome type 1	HP:0040283 - Occasional	173
HP:0000738	HP:0000738	Hallucinations	0	USH1G CL E G H	124590	16356	ORPHA:231169	Usher syndrome type 1	HP:0040283 - Occasional	78
HP:0000738	HP:0000738	Hallucinations	0	USH2A CL E G H	7399	12601	ORPHA:231178	Usher syndrome type 2	HP:0040283 - Occasional	777
HP:0000738	HP:0000738	Hallucinations	0	VCP CL E G H	7415	12666	ORPHA:275872	Frontotemporal dementia with motor neuron disease	HP:0040282 - Frequent	63
HP:0000738	HP:0000738	Hallucinations	0	VPS13C CL E G H	54832	23594	ORPHA:2828	Young-onset Parkinson disease	HP:0040282 - Frequent	8
HP:0000738	HP:0000738	Hallucinations	0	VPS35 CL E G H	55737	13487	ORPHA:411602	Hereditary late-onset Parkinson disease		37
HP:0000738	HP:0000738	Hallucinations	0	WFS1 CL E G H	7466	12762	ORPHA:3463	Wolfram syndrome	HP:0040283 - Occasional	389
HP:0000738	HP:0000738	Hallucinations	0	WHRN CL E G H	25861	16361	ORPHA:231178	Usher syndrome type 2	HP:0040283 - Occasional	155
HP:0000738	HP:0000738	Hallucinations	0	ZDHHC9 CL E G H	51114	18475	ORPHA:776	Lujan-Fryns syndrome	HP:0040283 - Occasional	10
HP:0000738	HP:0000738	Hallucinations	0	ZNF365 CL E G H	22891	18194	ORPHA:2073	Narcolepsy type 1	HP:0040281 - Very frequent	3
HP:0000738	HP:0000738	Hallucinations	0	ZNF365 CL E G H	22891	18194	ORPHA:83465	Narcolepsy type 2	HP:0040281 - Very frequent	3
HP:0000738	HP:0033694	Tactile hallucination	1	CL E G H
HP:0000738	HP:0006803	Vivid hallucinations	1	CL E G H
HP:0000738	HP:0002367	Visual hallucinations	1	ATP13A2 CL E G H	23400	30213	ORPHA:306674	Kufor-Rakeb syndrome	HP:0040282 - Frequent	100
HP:0000738	HP:0002367	Visual hallucinations	1	CACNA1A CL E G H	773	1388	OMIM:141500	Migraine, familial hemiplegic, 1	.	449
HP:0000738	HP:0008765	Auditory hallucinations	1	CACNA1A CL E G H	773	1388	OMIM:141500	Migraine, familial hemiplegic, 1	.	449
HP:0000738	HP:0008765	Auditory hallucinations	1	CDH2 CL E G H	1000	1759	OMIM:618929	AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME; ACOGS
HP:0000738	HP:0008765	Auditory hallucinations	1	CEP85L CL E G H	387119	21638	OMIM:618873	LISSENCEPHALY 10; LIS10		1
HP:0000738	HP:0002367	Visual hallucinations	1	CLN3 CL E G H	1201	2074	ORPHA:228346	CLN3 disease		216
HP:0000738	HP:0002367	Visual hallucinations	1	CLN6 CL E G H	54982	2077	OMIM:204300	Ceroid lipofuscinosis, neuronal, 4A, autosomal recessive	.	143
HP:0000738	HP:0008765	Auditory hallucinations	1	CLN6 CL E G H	54982	2077	OMIM:204300	Ceroid lipofuscinosis, neuronal, 4A, autosomal recessive	.	143
HP:0000738	HP:0008765	Auditory hallucinations	1	CSF1R CL E G H	1436	2433	OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		149
HP:0000738	HP:0002367	Visual hallucinations	1	DEPDC5 CL E G H	9681	18423	ORPHA:101046	Autosomal dominant epilepsy with auditory features	HP:0040283 - Occasional	172
HP:0000738	HP:0008765	Auditory hallucinations	1	DEPDC5 CL E G H	9681	18423	ORPHA:101046	Autosomal dominant epilepsy with auditory features	HP:0040281 - Very frequent	172
HP:0000738	HP:0008765	Auditory hallucinations	1	DEPDC5 CL E G H	9681	18423	ORPHA:98820	Familial focal epilepsy with variable foci	HP:0040283 - Occasional	172
HP:0000738	HP:0002367	Visual hallucinations	1	DEPDC5 CL E G H	9681	18423	ORPHA:98820	Familial focal epilepsy with variable foci	HP:0040283 - Occasional	172
HP:0000738	HP:0002367	Visual hallucinations	1	DNAJC13 CL E G H	23317	30343	ORPHA:411602	Hereditary late-onset Parkinson disease	HP:0040283 - Occasional	2
HP:0000738	HP:0008765	Auditory hallucinations	1	DNAJC5 CL E G H	80331	16235	OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant	.	155
HP:0000738	HP:0002367	Visual hallucinations	1	DNAJC5 CL E G H	80331	16235	OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant	.	155
HP:0000738	HP:0002367	Visual hallucinations	1	EIF4G1 CL E G H	1981	3296	ORPHA:411602	Hereditary late-onset Parkinson disease	HP:0040283 - Occasional	2
HP:0000738	HP:0002367	Visual hallucinations	1	EPM2A CL E G H	7957	3413	ORPHA:501	Lafora disease	HP:0040282 - Frequent	83
HP:0000738	HP:0002367	Visual hallucinations	1	EPM2A CL E G H	7957	3413	OMIM:254780	Myoclonic epilepsy of lafora	.	83
HP:0000738	HP:0002367	Visual hallucinations	1	FBXO7 CL E G H	25793	13586	ORPHA:171695	Parkinsonian-pyramidal syndrome	HP:0040282 - Frequent	36
HP:0000738	HP:0002367	Visual hallucinations	1	FIG4 CL E G H	9896	16873	ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria	HP:0040283 - Occasional	111
HP:0000738	HP:0008765	Auditory hallucinations	1	FIG4 CL E G H	9896	16873	ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria	HP:0040283 - Occasional	111
HP:0000738	HP:0002367	Visual hallucinations	1	FIG4 CL E G H	9896	16873	OMIM:612691	Polymicrogyria, bilateral temporooccipital	.	111
HP:0000738	HP:0002367	Visual hallucinations	1	GBA1 CL E G H	2629	4177	OMIM:127750	Dementia, lewy body	.
HP:0000738	HP:0002367	Visual hallucinations	1	GBA1 CL E G H	2629	4177	ORPHA:411602	Hereditary late-onset Parkinson disease	HP:0040283 - Occasional
HP:0000738	HP:0002367	Visual hallucinations	1	GIGYF2 CL E G H	26058	11960	ORPHA:411602	Hereditary late-onset Parkinson disease	HP:0040283 - Occasional	8
HP:0000738	HP:0006896	Hypnopompic hallucinations	1	HCRT CL E G H	3060	4847	OMIM:161400	Narcolepsy 1	.	1
HP:0000738	HP:0002519	Hypnagogic hallucinations	1	HCRT CL E G H	3060	4847	OMIM:161400	Narcolepsy 1	.	1
HP:0000738	HP:0002367	Visual hallucinations	1	LGI1 CL E G H	9211	6572	ORPHA:101046	Autosomal dominant epilepsy with auditory features	HP:0040283 - Occasional	75
HP:0000738	HP:0008765	Auditory hallucinations	1	LGI1 CL E G H	9211	6572	ORPHA:101046	Autosomal dominant epilepsy with auditory features	HP:0040281 - Very frequent	75
HP:0000738	HP:0002367	Visual hallucinations	1	LRRK2 CL E G H	120892	18618	ORPHA:411602	Hereditary late-onset Parkinson disease	HP:0040283 - Occasional	221
HP:0000738	HP:0008765	Auditory hallucinations	1	MMACHC CL E G H	25974	24525	ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC	HP:0040283 - Occasional	101
HP:0000738	HP:0002367	Visual hallucinations	1	NHLRC1 CL E G H	378884	21576	ORPHA:501	Lafora disease	HP:0040282 - Frequent	77
HP:0000738	HP:0002367	Visual hallucinations	1	NHLRC1 CL E G H	378884	21576	OMIM:254780	Myoclonic epilepsy of lafora	.	77
HP:0000738	HP:0002367	Visual hallucinations	1	NPRL2 CL E G H	10641	24969	ORPHA:98820	Familial focal epilepsy with variable foci	HP:0040283 - Occasional	4
HP:0000738	HP:0008765	Auditory hallucinations	1	NPRL2 CL E G H	10641	24969	ORPHA:98820	Familial focal epilepsy with variable foci	HP:0040283 - Occasional	4
HP:0000738	HP:0002367	Visual hallucinations	1	NPRL3 CL E G H	8131	14124	ORPHA:98820	Familial focal epilepsy with variable foci	HP:0040283 - Occasional	7
HP:0000738	HP:0008765	Auditory hallucinations	1	NPRL3 CL E G H	8131	14124	ORPHA:98820	Familial focal epilepsy with variable foci	HP:0040283 - Occasional	7
HP:0000738	HP:0002367	Visual hallucinations	1	PUS3 CL E G H	83480	25461	ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome	HP:0040283 - Occasional	1
HP:0000738	HP:0002367	Visual hallucinations	1	RELN CL E G H	5649	9957	ORPHA:101046	Autosomal dominant epilepsy with auditory features	HP:0040283 - Occasional	334
HP:0000738	HP:0008765	Auditory hallucinations	1	RELN CL E G H	5649	9957	ORPHA:101046	Autosomal dominant epilepsy with auditory features	HP:0040281 - Very frequent	334
HP:0000738	HP:0002367	Visual hallucinations	1	SNCA CL E G H	6622	11138	OMIM:127750	Dementia, lewy body	.	65
HP:0000738	HP:0002367	Visual hallucinations	1	SNCA CL E G H	6622	11138	ORPHA:411602	Hereditary late-onset Parkinson disease	HP:0040283 - Occasional	65
HP:0000738	HP:0002367	Visual hallucinations	1	SNCA CL E G H	6622	11138	ORPHA:171695	Parkinsonian-pyramidal syndrome	HP:0040282 - Frequent	65
HP:0000738	HP:0002367	Visual hallucinations	1	SNCB CL E G H	6620	11140	OMIM:127750	Dementia, lewy body	.	2
HP:0000738	HP:0008765	Auditory hallucinations	1	SON CL E G H	6651	11183	ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome	HP:0040283 - Occasional	12
HP:0000738	HP:0002367	Visual hallucinations	1	VPS35 CL E G H	55737	13487	ORPHA:411602	Hereditary late-onset Parkinson disease	HP:0040283 - Occasional	37