Search Ontology:
Human Disease

primary autosomal recessive microcephaly 3

Term ID
DOID:0070286
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models