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 ...