ZFIN Human Disease: Leber congenital amaurosis 8

OBO ID: DOID:0110079

Term Name:	Leber congenital amaurosis 8		Search Ontology:
Synonyms:	LCA8
Definition:	A Leber congenital amaurosis that is characterized by night blindness and thick unlaminated retinas and has_material_basis_in mutation in the CRB1 gene on chromosome 1q31-q32. https://www.ncbi.nlm.nih.gov/pubmed/11231775
References:	ICD10CM:H35.5 OMIM:613835
Ontology:	Human Disease ( DOID:0110079 )

Relationships

is a type of:	autosomal recessive disease Leber congenital amaurosis autosomal recessive disease Leber congenital amaurosis Show first 5 Terms

OTHER Leber congenital amaurosis 8 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CRB1	crb1	Leber congenital amaurosis 8	613835

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None