Disease #00209 (FFI (insomnia, fatal, familial), OMIM:600072)
| Official abbreviation |
FFI |
| Name |
insomnia, fatal, familial |
| OMIM ID |
600072 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
PRNP |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-09-24 21:04:17 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|