Visualize Submit Comment
Metadata
ID DOID:0070295
Name primary autosomal dominant microcephaly 18
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
Xrefs

MIM:617520

Synonyms

MCPH18 [EXACT]

Parent Relationships

is_a primary microcephaly

is_a autosomal dominant disease

Add an item to the term tracker