Search Ontology:
Human Disease

primary autosomal dominant microcephaly 18

Term ID
DOID:0070295
Synonyms
  • MCPH18
Definition
A primary microcephaly that has_material_basis_in heterozygous mutation in the WDFY3 gene on chromosome 4q21. https://www.ncbi.nlm.nih.gov/pubmed/27008544
References
Ontology
Human Disease   ( DOID:0070295 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models