ZFIN Human Disease: Leber congenital amaurosis 14

OBO ID: DOID:0110188

Term Name:	Leber congenital amaurosis 14		Search Ontology:
Synonyms:	LCA14
Definition:	A Leber congenital amaurosis that has_material_basis_in mutation in the LRAT gene on chromosome 4q31. https://www.ncbi.nlm.nih.gov/pubmed/17011878
References:	ICD10CM:H35.5 MESH:C567636 OMIM:613341
Ontology:	Human Disease ( DOID:0110188 )

Relationships

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

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
LRAT	lratb.1 lrata	Leber congenital amaurosis 14	613341
		Retinitis pigmentosa, juvenile	613341
		Retinal dystrophy, early-onset severe	613341

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None