OBO ID: DOID:0110079
Term Name: Leber congenital amaurosis 8 Search Ontology:
Synonyms:
  • LCA8
Definition: A Leber congenital amaurosis that is characterized by night blindness and thick unlaminated retinas and has_material_basis_in mutation in the CRB1 gene on chromosome 1q31-q32. https://www.ncbi.nlm.nih.gov/pubmed/11231775
References:
Ontology: Human Disease   (DOID:0110079)
OTHER Leber congenital amaurosis 8 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CRB1 Leber congenital amaurosis 8 613835
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None