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
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