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DO Term : Usher syndrome type 1G [DOID:0110834] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25.

synonyms:
Usher syndrome type IG,
ICD10CM:H35.5,
606943,
OMIM:606943,
USH1G

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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