OBO ID: DOID:0110217
Term Name: Leber congenital amaurosis 17 Search Ontology:
Synonyms:
  • LCA17
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the GDF6 gene on chromosome 8q22. https://www.ncbi.nlm.nih.gov/pubmed/23307924
References:
Ontology: Human Disease   (DOID:0110217)
OTHER Leber congenital amaurosis 17 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GDF6 Leber congenital amaurosis 17 615360
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None