Human Phenotype Ontology

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Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Hemianopia (HP:0012377)

Parent Node:
Heteronymous hemianopia (HP:0030517)

..Starting node
..Bitemporal hemianopia (HP:0030521)

Term ID:

30521

Name:

Bitemporal hemianopia

Synonym:

Definition:

Comments:

Reference:

HP:0030521

Genes and Diseases:

Child Nodes:

Sister Nodes:

Binasal hemianopia (HP:0030520)

Congruous heteronymous hemianopia (HP:0030519)

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:0030521	HP:0030521	Bitemporal hemianopia	0	AIP CL E G H	9049	358	ORPHA:2965	Prolactinoma	HP:0040283 - Occasional	95
HP:0030521	HP:0030521	Bitemporal hemianopia	0	AKT1 CL E G H	207	391	ORPHA:2495	Meningioma	HP:0040282 - Frequent	54
HP:0030521	HP:0030521	Bitemporal hemianopia	0	BAP1 CL E G H	8314	950	ORPHA:2495	Meningioma	HP:0040282 - Frequent	184
HP:0030521	HP:0030521	Bitemporal hemianopia	0	BRAF CL E G H	673	1097	ORPHA:54595	Craniopharyngioma	HP:0040282 - Frequent	276
HP:0030521	HP:0030521	Bitemporal hemianopia	0	CDH23 CL E G H	64072	13733	ORPHA:2965	Prolactinoma	HP:0040283 - Occasional	636
HP:0030521	HP:0030521	Bitemporal hemianopia	0	CDH23 CL E G H	64072	13733	ORPHA:91347	TSH-secreting pituitary adenoma	HP:0040283 - Occasional	636
HP:0030521	HP:0030521	Bitemporal hemianopia	0	CTNNB1 CL E G H	1499	2514	ORPHA:54595	Craniopharyngioma	HP:0040282 - Frequent	88
HP:0030521	HP:0030521	Bitemporal hemianopia	0	MEN1 CL E G H	4221	7010	ORPHA:2965	Prolactinoma	HP:0040283 - Occasional	462
HP:0030521	HP:0030521	Bitemporal hemianopia	0	NF2 CL E G H	4771	7773	ORPHA:2495	Meningioma	HP:0040282 - Frequent	220
HP:0030521	HP:0030521	Bitemporal hemianopia	0	PDGFB CL E G H	5155	8800	ORPHA:2495	Meningioma	HP:0040282 - Frequent	9
HP:0030521	HP:0030521	Bitemporal hemianopia	0	PIK3CA CL E G H	5290	8975	ORPHA:2495	Meningioma	HP:0040282 - Frequent	162
HP:0030521	HP:0030521	Bitemporal hemianopia	0	SMARCB1 CL E G H	6598	11103	ORPHA:2495	Meningioma	HP:0040282 - Frequent	87
HP:0030521	HP:0030521	Bitemporal hemianopia	0	SMARCE1 CL E G H	6605	11109	ORPHA:2495	Meningioma	HP:0040282 - Frequent	47
HP:0030521	HP:0030521	Bitemporal hemianopia	0	SMO CL E G H	6608	11119	ORPHA:2495	Meningioma	HP:0040282 - Frequent	22
HP:0030521	HP:0030521	Bitemporal hemianopia	0	SUFU CL E G H	51684	16466	ORPHA:2495	Meningioma	HP:0040282 - Frequent	124
HP:0030521	HP:0030521	Bitemporal hemianopia	0	TERT CL E G H	7015	11730	ORPHA:2495	Meningioma	HP:0040282 - Frequent	238
HP:0030521	HP:0030521	Bitemporal hemianopia	0	TRAF7 CL E G H	84231	20456	ORPHA:2495	Meningioma	HP:0040282 - Frequent

Genes (16) :AIP AKT1 BAP1 BRAF CDH23 CTNNB1 MEN1 NF2 PDGFB PIK3CA SMARCB1 SMARCE1 SMO SUFU TERT TRAF7

Diseases (4) :ORPHA:2965 ORPHA:2495 ORPHA:54595 ORPHA:91347

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.

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