OBO ID: DOID:0110080
Term Name: Leber congenital amaurosis 12 Search Ontology:
Synonyms:
  • LCA12
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the RD3 gene on chromosome 1q32. https://www.ncbi.nlm.nih.gov/pubmed/17186464
References:
Ontology: Human Disease   ( DOID:0110080 )
OTHER Leber congenital amaurosis 12 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
RD3 Leber congenital amaurosis 12 610612
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None