WormBase Tree Display for DO_term: DOID:0110333

DOID:0110333 Name: Leber congenital amaurosis 7
  Status: Valid
  Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the CRX gene on chromosome 19q13.
  Synonym: Exact: LCA7
  Parent: Is_a: DOID:14791
      DOID:0050177
  DB_info: Database: OMIM disease 613829
  Attribute_of: Gene_by_orthology: WBGene00000458