ZFIN Human Disease: Leber congenital amaurosis 11

OBO ID: DOID:0110216

OBO ID: DOID:0110216

Term Name:	Leber congenital amaurosis 11	Search Ontology:
Synonyms:	LCA11
Definition:	A Leber congenital amaurosis that has_material_basis_in mutation n the IMPDH1 gene on chromosome 7q31.3-q32. https://www.ncbi.nlm.nih.gov/pubmed/16384941
References:	ICD10CM:H35.5 MESH:C564140 OMIM:613837
Ontology:	Human Disease ( DOID:0110216 )

Relationships

is a type of:	autosomal dominant disease Leber congenital amaurosis autosomal dominant 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
IMPDH1	impdh1a impdh1b	Leber congenital amaurosis 11	613837

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None