OBO ID: DOID:0070285
Term Name: primary autosomal recessive microcephaly 1 Search Ontology:
Synonyms:
  • MCPH1
Definition: A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the MCPH1 gene on chromosome 8p23. https://www.ncbi.nlm.nih.gov/pubmed/12046007
References:
Ontology: Human Disease   (DOID:0070285)
OTHER primary autosomal recessive microcephaly 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MCPH1 Microcephaly 1, primary, autosomal recessive 251200
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None