WormBase Tree Display for DO_term: DOID:0070094

DOID:0070094 Name: oculocutaneous albinism type IA
  Status: Valid
  Definition: An oculocutaneous albinism that has_material_basis_in an autosomal recessive null mutation of TYR on chromosome 11q14.3 with no residual protein activity.
  Synonym: Exact (2)
  Parent: Is_a: DOID:0050632
  DB_info: Database: OMIM disease 203100
  Attribute_of: Gene_by_orthology (5)