Search Ontology:
Human Disease

primary autosomal recessive microcephaly 7

Term ID
DOID:0070278
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models