Human genes for MEHMO syndrome
MEHMO syndrome [DOID:0060801]
A syndromic X-linked intellectual disability characterized by severe intellectual deficit, epilepsy, microcephaly, hypogenitalism and obesity with variable occurrence of growth delay and diabetes that has_material_basis_in variation in the chromosome region Xp22.13-p21.1.
Synonyms: MEHMO syndrome, DOID:0060801, MEHMO disease, MEHMO disorder, MEHMO syndromes ...