WormBase Tree Display for DO_term: DOID:0110270

DOID:0110270 Name: cataract 17 multiple types
  Status: Valid
  Definition: A cataract that has_material_basis_in heterozygous or homozygous mutation in the beta-B1 crystallin gene (CRYBB1) on chromosome 22q12.
  Synonym: Exact: CTRCT17
    Narrow: CATCN3
      autosomal recessive congenital nuclear cataract 3
  Parent: Is_a: DOID:83
      DOID:0050736
      DOID:0050737
  DB_info: Database: OMIM disease 611544