Phenotype #0000204016
| Individual ID |
00266240 |
| Associated disease |
CMTX5 |
| Phenotype details |
hearing loss, epilepsy, peripheral neuropathy, severe IUGR |
| Diagnosis/Initial |
- |
| Inheritance |
Isolated (sporadic) |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
00y06m |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Laurence Jonard |
| Database submission license |
No license selected |
| Created by |
Laurence Jonard |
| Date created |
2019-10-17 16:40:37 +02:00 (CEST) |
| Date last edited |
2019-10-18 15:08:11 +02:00 (CEST) |
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