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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