Phenotype #0000210547
| Individual ID |
00275992 |
| Associated disease |
neuropathy, optic |
| Phenotype details |
Amblyopia (HP:0000646); Esodeviation (HP:0020045); Nystagmus (HP:0000639) |
| Diagnosis/Initial |
- |
| Diagnosis/Definite |
- |
| Inheritance |
Familial, autosomal dominant |
| Age/Examination |
08y (8 years) |
| Age/Diagnosis |
- |
| Age/Onset |
00y |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Khadidja Guehlouz |
| Database submission license |
No license selected |
| Created by |
Khadidja Guehlouz |
| Date created |
2020-01-22 12:06:54 +01:00 (CET) |
| Date last edited |
2020-08-25 21:27:59 +02:00 (CEST) |
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