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DO Term : Usher syndrome type 1B [DOID:0070655] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the MYO7A gene on chromosome 11q13.

synonyms:
USH1B,
UMLS_CUI:C2931206,
Usher syndrome type IB,
276900,
OMIM:276900,
MESH:C536485

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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