Harrod syndrome

MONDO:0010993

Harrod syndrome 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: Harrod syndrome, cranio-facio-digito-genital syndrome, Harrod Doman Keele syndrome, craniofacial digital genital anomalies

0 clinical trials for this condition and its sub-types, 0 tagged with Harrod syndrome itself.

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Part of

↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59)

Including sub-types (0) Tagged with Harrod syndrome (0)

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