OBO ID: DOID:0070278
Term Name: primary autosomal recessive microcephaly 7 Search Ontology:
Synonyms:
  • MCPH7
Definition: A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the STIL gene on chromosome 1p33. https://www.ncbi.nlm.nih.gov/pubmed/19215732
References:
Ontology: Human Disease   (DOID:0070278)
OTHER primary autosomal recessive microcephaly 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
STIL Microcephaly 7, primary, autosomal recessive 612703
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None