WormBase Tree Display for DO_term: DOID:0070288

DOID:0070288 Name: primary autosomal recessive microcephaly 17
  Status: Valid
  Definition: A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CIT gene on chromosome 12q24.
  Synonym: Exact: MCPH17
  Parent: Is_a: DOID:0070296
  DB_info: Database: OMIM disease 617090
  Attribute_of: Gene_by_orthology: WBGene00019087