syndromic disease SCARF syndrome https://www.malacards.org/card/scarf_syndrome Orphanet:3134 icd11.foundation:1075253748 MONDO:0010728 SCTID:734173003 UMLS:C1839321 A syndrome characterized by the association of skeletal abnormalities, cutis laxa, craniostenosis, ambiguous genitalia, psychomotor retardation and facial abnormalities. So far, it has been described in two males (maternal first cousins). The mode of inheritance was suggested to be X-linked recessive. skeletal abnormalities, cutis laxa, craniostenosis, ambiguous genitalia, retardation, and Facial abnormalities MESH:C536625 OMIM:312830 MEDGEN:326461 GARD:0000247 SCARF syndrome multiple congenital anomalies/dysmorphic syndrome-intellectual disability syndromic craniosynostosis X-linked syndromic intellectual disability inherited cutis laxa