Search Ontology:
Human Disease

primary autosomal recessive microcephaly 9

Term ID
DOID:0070292
Synonyms
  • MCPH9
Definition
A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21. https://www.ncbi.nlm.nih.gov/pubmed/20598275
References
Ontology
Human Disease   ( DOID:0070292 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models