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:
Ontology: Human Disease   (DOID:0110005)
OTHER Leber congenital amaurosis 9 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NMNAT1 Leber congenital amaurosis 9 608553
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None