Harrod syndrome (MONDO_0010993, a Monarch Disease Ontology entry) is characterized by the association of intellectual deficit, facial dysmorphism (a highly arched palate, pointed chin, and small mouth, hypotelorism, a long nose and large protruding ears), arachnodactyly, hypogenitalism (undescended testes and hypospadias) and failure to thrive. Also known as: cranio-facio-digito-genital syndrome.