Bardet-Biedl syndrome

Disease Export to PDF
Name:
Bardet-Biedl syndrome
Description:
A rare genetic multisystem disorder characterized by the variable association of retinal dystrophy, obesity, polydactyly, genitourinary and kidney anomalies, learning disability and hypogonadism, with a wide spectrum of other minor manifestations.
ORPHAcode:
110
Synonyms:
BBS
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14