Disease #01090 (HSN2C (neuropathy, sensory, hereditary, type IIC (HSN-2C)), OMIM:614213)
| Official abbreviation |
HSN2C |
| Name |
neuropathy, sensory, hereditary, type IIC (HSN-2C) |
| OMIM ID |
614213 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
9 |
| Phenotype entries for this disease |
9 |
| Associated with 1 gene |
KIF1A |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|