OBO ID: DOID:0110189
Term Name: Leber congenital amaurosis 15 Search Ontology:
Synonyms:
  • LCA15
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the TULP1 gene on chromosome 6p21.3. https://www.ncbi.nlm.nih.gov/pubmed/15024725
References:
Ontology: Human Disease   (DOID:0110189)
OTHER Leber congenital amaurosis 15 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TULP1 Leber congenital amaurosis 15 613843
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None