Human Phenotype Ontology

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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:
Constriction of peripheral visual field (HP:0001133)

..Starting node
..Very severe constriction of peripheral visual field (HP:0030527)

Term ID:

30527

Name:

Very severe constriction of peripheral visual field

Synonym:

Very severe peripheral visual field loss

Definition:

Peripheral visual field constriction with <10 degrees central field preserved.

Comments:

Reference:

HP:0030527

Genes and Diseases:

Child Nodes:

Sister Nodes:

Mild constriction of peripheral visual field (HP:0030522)

Moderate constriction of peripheral visual field (HP:0030525)

obsolete Peripheral visual field constriction with 30-39 degrees central field preserved (HP:0030524)

obsolete Peripheral visual field constriction with 40-50 degrees central field preserved (HP:0030523)

Peripheral visual field loss (HP:0007994)

Severe constriction of peripheral visual field (HP:0030526)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030527	HP:0030527	Very severe constriction of peripheral visual field	0	CL E G H

Genes (0) :

Diseases (0) :

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