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
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