DISEASES

Disease-gene associations mined from literature

Human genes for Armfield syndrome

Armfield syndrome [DOID:0050764]

A syndromic X-linked intellectual disability characterized by intellectual disability, short stature, seizures, and small hands and feet and in some cases cleft palate or cataracts/glaucoma that has_material_basis_in variation in the chromosomal region Xq28.

Synonyms:  Armfield syndrome,  Armfield disease,  Armfield disorder,  Armfield syndromes,  DOID:0050764 ...