OBO ID: DOID:0070292
Term Name: primary autosomal recessive microcephaly 9 Search Ontology:
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)
OTHER primary autosomal recessive microcephaly 9 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CEP152 Microcephaly 9, primary, autosomal recessive 614852
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None