ZFIN Human Disease: Leber congenital amaurosis 16

OBO ID: DOID:0110118

OBO ID: DOID:0110118

Term Name:	Leber congenital amaurosis 16	Search Ontology:
Synonyms:	LCA16
Definition:	A Leber congenital amaurosis that has_material_basis_in mutation in the KCNJ13 gene on chromosome 2q37. https://www.ncbi.nlm.nih.gov/pubmed/21763485
References:	ICD10CM:H35.5 OMIM:614186
Ontology:	Human Disease ( DOID:0110118 )

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 16 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
KCNJ13	kcnj13	Leber congenital amaurosis 16	614186

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None