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DO Term : Usher syndrome type 2C [DOID:0110839] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An Usher syndrome type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the ADGRV1 gene on chromosome 5q14.

synonyms:
Usher syndrome IIC,
605472,
ICD10CM:H35.5,
USH2C,
Usher syndrome type IIC,
OMIM:605472

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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