Monarch Disease Ontology id MONDO_0008711 (Goodman syndrome) is an extremely rare genetic disorder characterized by marked malformations of the head and face (essentially acrocephaly), abnormalities of the hands and feet (polydactyly, syndactyly, clinodactyly, camptodactyly, ulnar deviation), and congenital heart disease. There have been no further descriptions in the literature since 1979. Goodman syndrome could be a variant of Carpenter syndrome. Also known as: ACPS 4, ACPS4, acrocephalopolysyndactyly type 4.