Term Name: primary autosomal dominant microcephaly 18
Synonyms: MCPH18
Definition: A primary microcephaly that has_material_basis_in heterozygous mutation in the WDFY3 gene on chromosome 4q21.
Ontology: Human Disease [DOID:0070295]   ( DOID:0070295 )

Relationships
is a type of: autosomal dominant primary microcephaly