OBO ID: DOID:0070284
Term Name: primary autosomal recessive microcephaly 12 Search Ontology:
Synonyms:
  • MCPH12
Definition: A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CDK6 gene on chromosome 7q21. https://www.ncbi.nlm.nih.gov/pubmed/23918663
References:
Ontology: Human Disease   (DOID:0070284)
OTHER primary autosomal recessive microcephaly 12 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CDK6 ?Microcephaly 12, primary, autosomal recessive 616080
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None