OBO ID: DOID:0070295
Term Name: primary autosomal dominant microcephaly 18 Search Ontology:
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)
OTHER primary autosomal dominant microcephaly 18 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
WDFY3 ?Microcephaly 18, primary, autosomal dominant 617520
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None