syndromic disease Simpson-Golabi-Behmel syndrome https://rarediseases.info.nih.gov/diseases/7649/simpson-golabi-behmel-syndrome https://www.malacards.org/card/simpson_golabi_behmel_syndrome_type_1_2 Orphanet:373 X-linked dysplasia gigantism syndrome SDYS MONDO:0010731 SGBS ICD9:759.89 UMLS:C4317043 Simpson-Golabi-Behmel syndrome NORD:1717 SCTID:439143004 MESH:C537340 SGB syndrome DGSX Sara Angers syndrome Golabi-Rosen syndrome icd11.foundation:181316558 Simpson-Golabi-Behmel syndrome is a rare X-linked multiple congenital anomalies syndrome, characterized by pre- and postnatal overgrowth, distinctive craniofacial features, variable congenital malformations, organomegaly and an increased tumor risk. MEDGEN:1387611 NCIT:C131002 GARD:0007649 NANDO:2200978 multiple congenital anomalies/dysmorphic syndrome-intellectual disability obsolete syndromic diaphragmatic or abdominal wall malformation macroglossia obsolete syndrome or malformation associated with head and neck malformations obsolete syndromic diaphragmatic or thoracic malformation overgrowth syndrome obsolete syndromic renal or urinary tract malformation X-linked syndromic intellectual disability