Disease #05122 (HSN (neuropathy, sensory, hereditary (HSN)))
| Official abbreviation |
HSN |
| Name |
neuropathy, sensory, hereditary (HSN) |
| OMIM ID |
- |
| Inheritance |
- |
| Individuals reported having this disease |
14 |
| Phenotype entries for this disease |
14 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2016-01-24 01:36:12 +01:00 (CET) |
| Date last edited |
2020-04-22 19:42:45 +02:00 (CEST) |
Individuals
|