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:
Abnormality of vision (HP:0000504)

Parent Node:
Visual impairment (HP:0000505)

..Starting node
..obsolete Congenital visual impairment (HP:0007758)

Term ID:

7758

Name:

obsolete Congenital visual impairment

Synonym:

Definition:

Comments:

Reference:

HP:0007758

Genes and Diseases:

Child Nodes:

Sister Nodes:

Blindness (HP:0000618)

Cerebral visual impairment (HP:0100704)

Moderately reduced visual acuity (HP:0030515)

Severely reduced visual acuity (HP:0001141)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007758	HP:0007758	obsolete Congenital visual impairment	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.