Disease #00089 (BBS1 (Bardet-Biedl syndrome, type 1 (BBS-1)), OMIM:209900)
Official abbreviation |
BBS1 |
Name |
Bardet-Biedl syndrome, type 1 (BBS-1) |
OMIM ID |
209900 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive, Digenic recessive |
Individuals reported having this disease |
12 |
Phenotype entries for this disease |
11 |
Associated with 4 genes |
BBS1, CCDC28B, MKS1, TMEM67 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2012-11-26 09:02:23 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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