Disease #02413 (USH-1F (Usher syndrome, type 1F (USH-1F)), OMIM:602083)

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Official abbreviation	USH-1F
Name	Usher syndrome, type 1F (USH-1F)
OMIM ID	602083
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PCDH15
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A