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Metadata
ID	DOID:0110832
Name	Usher syndrome type 1F
Definition	An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the PCDH15 gene on chromosome 10q. https://www.ncbi.nlm.nih.gov/pubmed/11398101
Xrefs	ICD10CM:H35.5 OMIM:602083
Synonyms	USH1F [EXACT] Usher syndrome type IF [EXACT]
Parent Relationships	is_a Usher syndrome type 1