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DO Term : Usher syndrome type 1C [DOID:0110830] 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 USH1C gene on chromosome 11p15.
  • synonyms:
  • Usher syndrome type I Acadian variety,
  • Usher syndrome type IC,
  • USH1C,
  • OMIM:276904,
  • ICD10CM:H35.5,
  • 276904
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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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