OBO ID: DOID:0070287
Term Name: primary autosomal recessive microcephaly 11 Search Ontology:
Synonyms:
  • MCPH11
Definition: A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the PHC1 gene on chromosome 12p13. https://www.ncbi.nlm.nih.gov/pubmed/23418308
References:
Ontology: Human Disease   (DOID:0070287)
OTHER primary autosomal recessive microcephaly 11 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PHC1 ?Microcephaly 11, primary, autosomal recessive 615414
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None