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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 MIM:276902
Synonyms	USH3A [EXACT] Usher syndrome type IIIA [EXACT]
Parent Relationships	is_a Usher syndrome type 3