WormBase Tree Display for DO_term: DOID:0110007

DOID:0110007 Name: achromatopsia 2
  Status: Valid
  Definition: An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11.
  Synonym: Exact (4)
  Parent: Is_a (2)
  DB_info: Database: OMIM disease 216900
  Attribute_of: Gene_by_orthology (3)