Disease #06618 (BDA1D (Brachydactyly, type A1, D), OMIM:616849)
Official abbreviation |
BDA1D |
Name |
Brachydactyly, type A1, D |
OMIM ID |
616849 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
BMPR1B |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
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