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DO Term : Usher syndrome type 1F [DOID:0110832] 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 PCDH15 gene on chromosome 10q.

synonyms:
ICD10CM:H35.5,
Usher syndrome type IF,
USH1F,
OMIM:602083,
602083

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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