X-linked intellectual disability-craniofacioskeletal syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/5588 https://www.malacards.org/card/craniofacioskeletal_syndrome https://www.malacards.org/card/x_linked_intellectual_disability_craniofacioskeletal_syndrome_2 craniofacioskeletal syndrome, X-linked recessive, X-linked dominant MONDO:0010412 craniofacioskeletal syndrome GARD:0017009 MEDGEN:394716 OMIM:300712 UMLS:C2678036 MESH:C567471 Orphanet:163979 X-linked intellectual disability-craniofacioskeletal syndrome is a rare, hereditary, syndromic intellectual disability characterized by craniofacial and skeletal abnormalities in association with mild intellectual disability in females and early postnatal lethality in males. In addition to mild cognitive impairment, females present with microcephaly, short stature, skeletal features and extra temporal lobe gyrus. In males, intrauterine growth impairment, cardiac and urogenital anomalies have been reported. X-linked syndromic intellectual disability