Disease #00218 (IBMPFD (myopathy, inclusion body, with early-onset Paget disease and frontotemporal dementia (IBMPFD)), OMIM:167320)
| Official abbreviation |
IBMPFD |
| Name |
myopathy, inclusion body, with early-onset Paget disease and frontotemporal dementia (IBMPFD) |
| OMIM ID |
167320 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
VCP |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-10-02 11:35:03 +02:00 (CEST) |
| Date last edited |
N/A |
|
