Search Ontology:
Human Disease

primary autosomal recessive microcephaly 13

Term ID
DOID:0070283
Synonyms
  • MCPH13
Definition
A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CENPE gene on chromosome 4q24. https://www.ncbi.nlm.nih.gov/pubmed/24748105
References
Ontology
Human Disease   ( DOID:0070283 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models