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Metadata
ID	DOID:0110830
Name	Usher syndrome type 1C
Definition	An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15. https://www.ncbi.nlm.nih.gov/pubmed/10973247
Xrefs	ICD10CM:H35.5 OMIM:276904
Synonyms	USH1C [EXACT] Usher syndrome type I Acadian variety [EXACT] Usher syndrome type IC [EXACT]
Parent Relationships	is_a Usher syndrome type 1