Disease #01856 (PDB-5 (Paget disease of bone, type 5, juvenile-onset (PDB-5, hyperphosphatasia)), OMIM:239000)
| Official abbreviation |
PDB-5 |
| Name |
Paget disease of bone, type 5, juvenile-onset (PDB-5, hyperphosphatasia) |
| OMIM ID |
239000 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
TNFRSF11B |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
