Harrod syndrome

Orpha code: 2115OMIM code: 601095

Definition

A rare multiple congenital anomalies/dysmorphic syndrome 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.

Disease data
Classification

Malformation syndrome

Synonyms
Cranio-facio-digito-genital syndrome
Zespół czaszkowo-twarzowo-palcowo-płciowy
ORPHA code
2115
OMIM code
601095
ICD10 code
Q87.8
ICD11 code
-

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl