DISEASES

Disease-gene associations mined from literature

Human genes for primary autosomal dominant microcephaly 18

Primary autosomal dominant microcephaly 18 [DOID:0070295]

A primary microcephaly that has_material_basis_in heterozygous mutation in the WDFY3 gene on chromosome 4q21.

Synonyms:  primary autosomal dominant microcephaly 18,  DOID:0070295,  MCPH18