ZFIN Human Disease: Leber congenital amaurosis 9

OBO ID: DOID:0110005

OBO ID: DOID:0110005

Term Name:	Leber congenital amaurosis 9	Search Ontology:
Synonyms:	LCA9
Definition:	A Leber congenital amaurosis that has_material_basis_in mutation in the NMNAT1 gene on chromosome 1p36. https://www.ncbi.nlm.nih.gov/pubmed/22842230
References:	ICD10CM:H35.5 OMIM:608553
Ontology:	Human Disease ( DOID:0110005 )

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 9 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NMNAT1	nmnat1	Leber congenital amaurosis 9	608553

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None