WormBase Tree Display for DO_term: DOID:0110714

DOID:0110714 Name: congenital stationary night blindness 1G
  Status: Valid
  Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the GNAT1 gene on chromosome 3p21.
  Synonym: Exact (2)
  Parent: Is_a (2)
  DB_info: Database: OMIM disease 616389
  Attribute_of: Gene_by_orthology (2)