OBO ID: DOID:0070291
Term Name: primary autosomal recessive microcephaly 4 Search Ontology:
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)
OTHER primary autosomal recessive microcephaly 4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
KNL1 Microcephaly 4, primary, autosomal recessive 604321
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None