DISEASES

Disease-gene associations mined from literature

Human genes for Xia-Gibbs Syndrome

Xia-Gibbs Syndrome [DOID:0070055]

An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of AHDC1 on chromosome 1p36.1-p35.3.

Synonyms:  Xia-Gibbs Syndrome,  DOID:0070055,  XiaGibbs Syndrome,  Xia-Gibbs disease,  Xia-Gibbs disorder ...