Search Ontology:
Human Disease

primary autosomal recessive microcephaly 4

Term ID
DOID:0070291
Synonyms
  • MCPH4
Definition
A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the KNL1 gene on chromosome 15q15. https://www.ncbi.nlm.nih.gov/pubmed/22983954
References
Ontology
Human Disease   ( DOID:0070291 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models