Disease #00179 (BDB1 (brachydactyly, type B1 (BDB1)), OMIM:113000)
| Official abbreviation |
BDB1 |
| Name |
brachydactyly, type B1 (BDB1) |
| OMIM ID |
113000 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
12 |
| Phenotype entries for this disease |
12 |
| Associated with 1 gene |
ROR2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-08-28 18:20:45 +02:00 (CEST) |
| Date last edited |
2020-09-29 10:08:02 +02:00 (CEST) |
Individuals
|