OBO ID: DOID:0110333
Term Name: Leber congenital amaurosis 7 Search Ontology:
Synonyms:
  • LCA7
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the CRX gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/9537410
References:
Ontology: Human Disease   ( DOID:0110333 )
Relationships
is a type of:
OTHER Leber congenital amaurosis 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CRX Leber congenital amaurosis 7 613829
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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