ZFIN Human Disease: Usher syndrome type 3

OBO ID: DOID:0110828

OBO ID: DOID:0110828

Term Name:	Usher syndrome type 3	Search Ontology:
Synonyms:	USH3
Definition:	An Usher syndrome characterized by progressive hearing loss typically beginning in late childhood, variable vestibular dysfunction and onset of retinitis pigmentosa by the second decade of life. (3)
References:	GARD:5442 MESH:D052245 NCI:C126329 ORDO:231183
Ontology:	Human Disease ( DOID:0110828 )

Relationships

is a type of:	Usher syndrome Usher syndrome Show first 5 Terms
has subtype:	Usher syndrome type 3A Usher syndrome type 3B Usher syndrome type 3A Usher syndrome type 3B Show first 5 Terms

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Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None