Phenotype #0000237154
| Individual ID |
00312025 |
| Associated disease |
neuropathy, optic |
| Phenotype details |
Optic atrophy (HP:0000648); Reduced visual acuity (HP:0007663); Developmental cataract (HP:0000519); Hearing impairment (HP:0000365); Abnormality of visual evoked potentials (HP:0000649); Abnormal electroretinogram (HP:0000512); Congenital hip dislocation (HP:0001374); |
| Diagnosis/Initial |
- |
| Diagnosis/Definite |
- |
| Inheritance |
Isolated (sporadic) |
| Age/Examination |
40y (40 years) |
| Age/Diagnosis |
- |
| Age/Onset |
? |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Benjamin Billiet |
| Database submission license |
No license selected |
| Created by |
Benjamin Billiet |
| Date created |
2020-09-30 11:06:22 +02:00 (CEST) |
| Date last edited |
2021-05-05 16:34:12 +02:00 (CEST) |
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