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:
Visual field defect (HP:0001123)

Parent Node:
Abnormal visual field test (HP:0030588)

..Starting node
..Abnormal kinetic perimetry test (HP:0030591)

Term ID:

30591

Name:

Abnormal kinetic perimetry test

Synonym:

Definition:

Comments:

Reference:

HP:0030591

Genes and Diseases:

Child Nodes:

........

Abnormal manual kinetic perimetry test (HP:0030593)

........

Abnormal automated kinetic perimetry test (HP:0030594)

Sister Nodes:

Abnormal Amsler grid test (HP:0030590)

Abnormal confrontational visual field test (HP:0030589)

Abnormal static perimetry test (HP:0030592)

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:0030591	HP:0030591	Abnormal kinetic perimetry test	0	AKT1 CL E G H	207	391	ORPHA:2495	Meningioma	HP:0040283 - Occasional	54
HP:0030591	HP:0030591	Abnormal kinetic perimetry test	0	BAP1 CL E G H	8314	950	ORPHA:2495	Meningioma	HP:0040283 - Occasional	184
HP:0030591	HP:0030591	Abnormal kinetic perimetry test	0	NF2 CL E G H	4771	7773	ORPHA:2495	Meningioma	HP:0040283 - Occasional	220
HP:0030591	HP:0030591	Abnormal kinetic perimetry test	0	PDGFB CL E G H	5155	8800	ORPHA:2495	Meningioma	HP:0040283 - Occasional	9
HP:0030591	HP:0030591	Abnormal kinetic perimetry test	0	PIK3CA CL E G H	5290	8975	ORPHA:2495	Meningioma	HP:0040283 - Occasional	162
HP:0030591	HP:0030591	Abnormal kinetic perimetry test	0	SMARCB1 CL E G H	6598	11103	ORPHA:2495	Meningioma	HP:0040283 - Occasional	87
HP:0030591	HP:0030591	Abnormal kinetic perimetry test	0	SMARCE1 CL E G H	6605	11109	ORPHA:2495	Meningioma	HP:0040283 - Occasional	47
HP:0030591	HP:0030591	Abnormal kinetic perimetry test	0	SMO CL E G H	6608	11119	ORPHA:2495	Meningioma	HP:0040283 - Occasional	22
HP:0030591	HP:0030591	Abnormal kinetic perimetry test	0	SUFU CL E G H	51684	16466	ORPHA:2495	Meningioma	HP:0040283 - Occasional	124
HP:0030591	HP:0030591	Abnormal kinetic perimetry test	0	TERT CL E G H	7015	11730	ORPHA:2495	Meningioma	HP:0040283 - Occasional	238
HP:0030591	HP:0030591	Abnormal kinetic perimetry test	0	TRAF7 CL E G H	84231	20456	ORPHA:2495	Meningioma	HP:0040283 - Occasional
HP:0030591	HP:0030593	Abnormal manual kinetic perimetry test	1	CL E G H
HP:0030591	HP:0030594	Abnormal automated kinetic perimetry test	1	CL E G H

Genes (11) :AKT1 BAP1 NF2 PDGFB PIK3CA SMARCB1 SMARCE1 SMO SUFU TERT TRAF7

Diseases (1) :ORPHA:2495

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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