syndromic X-linked intellectual disability 12 https://github.com/monarch-initiative/mondo/issues/5588 https://www.malacards.org/card/intellectual_developmental_disorder_x_linked_syndromic_12 https://www.malacards.org/card/syndromic_x_linked_intellectual_disability_12 OMIM:309545 MONDO:0010658 DOID:0060804 X-linked intellectual disability, Wilson type X-linked intellectual disability, Wilson type is characterized by severe intellectual deficit with mutism, epilepsy, growth retardation and recurrent infections. It has been described in three males from three generations of one family. The causative gene has been localized to the 11p region of the X chromosome. MEDGEN:333405 MESH:C564106 SCTID:719009006 MRXS12 syndromic X-linked intellectual disability type 12 UMLS:C1839792 GARD:0016747 mental retardation, X-linked, syndromic 12 Orphanet:85290 intellectual disability, X-linked, syndromic 12 X-linked syndromic intellectual disability