overgrowth syndrome overgrowth syndrome with 2q37 translocation https://github.com/monarch-initiative/mondo/issues/4948 https://www.malacards.org/card/overgrowth_syndrome_with_2q37_translocation UMLS:C5567236 MONDO:0034676 GARD:0022032 MEDGEN:1798659 Orphanet:498488 A rare overgrowth syndrome with skeletal involvement characterized by long and slim body habitus and multiple skeletal manifestations, such as scoliosis, macrodactyly of the big toes, arachnodactyly of fingers and toes, camptodactyly and clinodactyly, and progressive valgus deformities of the feet. Epimetaphyseal dysplasia, bowing of the tibiae, and dysmorphic facial features (hypertelorism, high palate, or micrognathia), as well as aortic root dilatation and umbilical hernia have also been reported.