WormBase Tree Display for DO_term: DOID:0070285

DOID:0070285 Name: primary autosomal recessive microcephaly 1
  Status: Valid
  Definition: A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the MCPH1 gene on chromosome 8p23.
  Synonym: Exact: MCPH1
  Parent: Is_a: DOID:0070296
  DB_info: Database: OMIM disease 251200
  Attribute_of: Gene_by_orthology: WBGene00012236