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Bardet-Biedl syndrome

rare

A 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

Also known as
BBS
Disease
  1. Bardet-Biedl syndrome 1 MONDO:0008854
  2. Bardet-Biedl syndrome 10 MONDO:0014438
  3. Bardet-Biedl syndrome 11 MONDO:0014439
  4. Bardet-Biedl syndrome 12 MONDO:0014440
  5. Bardet-Biedl syndrome 13 MONDO:0014441
  6. Bardet-Biedl syndrome 14 MONDO:0014442
  7. Bardet-Biedl syndrome 15 MONDO:0014443
  8. Bardet-Biedl syndrome 16 MONDO:0014444
  9. Bardet-Biedl syndrome 17 MONDO:0014445
  10. Bardet-Biedl syndrome 18 MONDO:0014446 BBIP1
  11. Bardet-Biedl syndrome 19 MONDO:0014447 IFT27
  12. Bardet-Biedl syndrome 2 MONDO:0014432
  13. Bardet-Biedl syndrome 20 MONDO:0023670 IFT172
  14. Bardet-Biedl syndrome 22 MONDO:0014926
  15. Bardet-Biedl syndrome 3 MONDO:0010832
  16. Bardet-Biedl syndrome 4 MONDO:0014433 BBS4
  17. Bardet-Biedl syndrome 5 MONDO:0014434
  18. Bardet-Biedl syndrome 6 MONDO:0011523
  19. Bardet-Biedl syndrome 7 MONDO:0014435
  20. Bardet-Biedl syndrome 8 MONDO:0014436
  21. Bardet-Biedl syndrome 9 MONDO:0014437
  22. Bardet-biedl syndrome 21 MONDO:0044308

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