Definition
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.
Definition
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.
Disease data
Classification
Disease
Synonyms
BBS
BBS
ORPHA code
110
OMIM code
617406
ICD10 code
Q87.8
ICD11 code
5A61.0
No additional description.
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