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DO Term : Usher syndrome type 2D [DOID:0110840] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An Usher syndrome type 2 that has_material_basis_in by homozygous or compound heterozygous mutation in the WHRN gene on chromosome 9q32.

synonyms:
OMIM:611383,
USH2D,
611383,
Usher syndrome type IID,
ICD10CM:H35.5

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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