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Bardet-Biedl syndrome
rareA ciliopathy with multisystem involvement. It is invariantly characterized by rod-cone dystrophy, and at least three additional non-ocular features such as intellectual disability, obesity, polydactyly, hypogonadism, or renal anomalies as primary manifestations. In the absence of one of these four primary clinical features, the diagnosis of BBS is made when at least two secondary features are observed, including hepatic fibrosis, diabetes mellitus, reproductive and developmental abnormalities, growth retardation, speech delays, or cardiovascular problems
- Identifiers
- MONDO:0015229 Orphanet:110
- Also known as
- BBS
Subtypes
Disease
- Bardet-Biedl syndrome 1 MONDO:0008854
- Bardet-Biedl syndrome 10 MONDO:0014438
- Bardet-Biedl syndrome 11 MONDO:0014439
- Bardet-Biedl syndrome 12 MONDO:0014440
- Bardet-Biedl syndrome 13 MONDO:0014441
- Bardet-Biedl syndrome 14 MONDO:0014442
- Bardet-Biedl syndrome 15 MONDO:0014443
- Bardet-Biedl syndrome 16 MONDO:0014444
- Bardet-Biedl syndrome 17 MONDO:0014445
- Bardet-Biedl syndrome 18 MONDO:0014446 BBIP1
- Bardet-Biedl syndrome 19 MONDO:0014447 IFT27
- Bardet-Biedl syndrome 2 MONDO:0014432
- Bardet-Biedl syndrome 20 MONDO:0023670 IFT172
- Bardet-Biedl syndrome 22 MONDO:0014926
- Bardet-Biedl syndrome 3 MONDO:0010832
- Bardet-Biedl syndrome 4 MONDO:0014433 BBS4
- Bardet-Biedl syndrome 5 MONDO:0014434
- Bardet-Biedl syndrome 6 MONDO:0011523
- Bardet-Biedl syndrome 7 MONDO:0014435
- Bardet-Biedl syndrome 8 MONDO:0014436
- Bardet-Biedl syndrome 9 MONDO:0014437
- Bardet-biedl syndrome 21 MONDO:0044308
Projects
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