Visualize Submit Comment
Metadata
ID DOID:0110841
Name Usher syndrome type 3A
Definition An Usher syndrome type 3 that has_material_basis_in homozygous or compound heterozygous mutation in the CLRN1 gene on chromosome 3q25.
https://www.ncbi.nlm.nih.gov/pubmed/11524702
Xrefs

ICD10CM:H35.5

OMIM:276902

Synonyms

USH3A [EXACT]

Usher syndrome type IIIA [EXACT]

Parent Relationships

is_a Usher syndrome type 3

Add an item to the term tracker