ZFIN Human Disease: Usher syndrome type 1

OBO ID: DOID:0110826

Term Name:	Usher syndrome type 1		Search Ontology:
Synonyms:	US1 USH1
Definition:	An Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa. (3)
References:	ICD10CM:H35.5 OMIM:276900 ORDO:231169
Ontology:	Human Disease ( DOID:0110826 )

Relationships

is a type of:	Usher syndrome Usher syndrome Show first 5 Terms
has subtype:	Usher syndrome type 1C Usher syndrome type 1D Usher syndrome type 1E Usher syndrome type 1F Usher syndrome type 1G ... Show All 8 Terms Usher syndrome type 1C Usher syndrome type 1D Usher syndrome type 1E Usher syndrome type 1F Usher syndrome type 1G Usher syndrome type 1H Usher syndrome type 1J Usher syndrome type 1K Show first 5 Terms

OTHER Usher syndrome type 1 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MYO7A	myo7ab myo7aa	Usher syndrome, type 1B	276900

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None