Autosomal dominant Robinow syndrome

Disease Export to PDF
Name:
Autosomal dominant Robinow syndrome
Description:
The more common type of Robinow syndrome (RS) characterized by mild to moderate limb shortening and abnormalities of the head, face and external genitalia.
ORPHAcode:
3107
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14