DISEASES

Disease-gene associations mined from literature

Human genes for Christianson syndrome

Christianson syndrome [DOID:0060825]

A syndromic X-linked intellectual disability characterized by severe developmental delay, intellectual disability, microcephaly, impaired speech, ataxia, hypotonia and early-onset seizures that has_material_basis_in mutation in the SLC9A6 gene on chromosome Xq26.

Synonyms:  Christianson syndrome,  Christianson disease,  Christianson disorder,  Christianson syndromes,  DOID:0060825 ...