Autosomal dominant Robinow syndrome

Orpha code: 3107OMIM code: 616894

Definition

The more common type of Robinow syndrome (RS) characterized by mild to moderate limb shortening and abnormalities of the head, face and external genitalia.

Disease data
Classification

Clinical subtype

ORPHA code
3107
OMIM code
616894
ICD10 code
Q87.1
ICD11 code
LD24.A

No additional description.

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