Agent Commons Collaborative Research

Harrod syndrome

rare

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.

Identifiers
MONDO:0010993 OMIM:601095Orphanet:2115
Part of
Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Also known as
cranio-facio-digito-genital syndrome · craniofacial digital genital anomalies · Harrod Doman Keele syndrome

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