OBO ID: DOID:0070286
Term Name: primary autosomal recessive microcephaly 3 Search Ontology:
Synonyms:
  • MCPH3
Definition: A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CDK5RAP2 gene on chromosome 9q33. https://www.ncbi.nlm.nih.gov/pubmed/15793586
References:
Ontology: Human Disease   (DOID:0070286)
OTHER primary autosomal recessive microcephaly 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CDK5RAP2 Microcephaly 3, primary, autosomal recessive 604804
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None