OBO ID: DOID:0110188
Term Name: Leber congenital amaurosis 14 Search Ontology:
Synonyms:
  • LCA14
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the LRAT gene on chromosome 4q31. https://www.ncbi.nlm.nih.gov/pubmed/17011878
References:
Ontology: Human Disease   (DOID:0110188)
OTHER Leber congenital amaurosis 14 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
LRAT Leber congenital amaurosis 14 613341
Retinitis pigmentosa, juvenile 613341
Retinal dystrophy, early-onset severe 613341
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None