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Usher syndrome type 3A

Go to external page http://purl.obolibrary.org/obo/DOID_0110841

An Usher syndrome type 3 that has_material_basis_in homozygous or compound heterozygous mutation in the CLRN1 gene on chromosome 3q25. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

Usher syndrome type 3A

Synonyms
  • USH3A
  • Usher syndrome type IIIA
database cross reference
has obo namespace

disease_ontology

id

DOID:0110841