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:
Ontology: Human Disease   (DOID:0110118)
OTHER Leber congenital amaurosis 16 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
KCNJ13 Leber congenital amaurosis 16 614186
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None