Phenotype #0000291911
| Individual ID |
00398816 |
| Associated disease |
CMT2O |
| Phenotype details |
Peripheral neuropathy (HP:0009830), Decreased nerve conduction velocity (HP:0000762) |
| Diagnosis/Initial |
CMT |
| Inheritance |
Unknown |
| Diagnosis/Definite |
- |
| Age/Examination |
63y (63 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Yvet den Hartog |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Yvet den Hartog |
| Date created |
2022-01-13 12:38:54 +01:00 (CET) |
| Date last edited |
2022-01-18 16:19:12 +01:00 (CET) |
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