Disease #00009 (FFI (Fatal Familial Insomnia), OMIM:600072)
| Official abbreviation |
FFI |
| Name |
Fatal Familial Insomnia |
| OMIM ID |
600072 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
8 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PRNP |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
Individuals
|
|