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Usher syndrome type 1C

Go to external page http://purl.obolibrary.org/obo/DOID_0110830

An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

Usher syndrome type 1C

Synonyms
  • USH1C
  • Usher syndrome type I Acadian variety
  • Usher syndrome type IC
database cross reference
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disease_ontology

id

DOID:0110830