congenital nervous system disorder multiple congenital anomalies/dysmorphic syndrome-intellectual disability X-linked intellectual disability, Pai type https://github.com/monarch-initiative/mondo/issues/5588 https://www.malacards.org/card/x_linked_intellectual_disability_pai_type SCTID:719011002 UMLS:C4305026 GARD:0019056 X-linked intellectual disability, Pai type is characterized by the association of dysmorphism with intellectual deficit. It has been described in four generations of one family. Premature death was reported in the affected males. Transmission is X-linked recessive and the causative gene has been localized to the q28 region of the X chromosome. Orphanet:85322 MEDGEN:930695 MONDO:0019420 X-linked syndromic intellectual disability