Disease #01034 (Fibular hypoplasia and complex brachydactyly, OMIM:228900)
Official abbreviation |
- |
Name |
Fibular hypoplasia and complex brachydactyly |
OMIM ID |
228900 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
GDF5 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
|