DISEASES

Disease-gene associations mined from literature

Human genes for syndromic X-linked intellectual disability Snyder type

Syndromic X-linked intellectual disability Snyder type [DOID:0060802]

A syndromic X-linked intellectual disability characterized by mild to profound intellectual disability, facial asymmetry, marfanoid habitus, asthenic habitus, unsteady gait, thickened lower lip, nasal dysarthic speech, narrow or cleft palate, osteoporosis, kyphoscoliosis, long great toes, short stature, pectus carinatum, and myopia that has_material_basis_in mutation in the SMS gene on chromosome Xp22.

Synonyms:  syndromic X-linked intellectual disability Snyder type,  DOID:0060802,  syndromic Xlinked intellectual disability Snyder type,  syndromic X-linked intellectual disability Snyder types,  SRS ...