Phenotype #0000238251
| Individual ID |
00313951 |
| Associated disease |
neuropathy, optic |
| Phenotype details |
Psychosis (HP:0000709); Optic atrophy (HP:0000648); Intellectual disability (HP:0001249); Seizure (HP:0001250); Decreased activity of mitochondrial complex I (HP:0011923) |
| Diagnosis/Initial |
- |
| Diagnosis/Definite |
- |
| Inheritance |
Unknown |
| Age/Examination |
32y (32 years) |
| Age/Diagnosis |
- |
| Age/Onset |
? |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Benjamin Billiet |
| Database submission license |
No license selected |
| Created by |
Benjamin Billiet |
| Date created |
2020-10-08 14:35:37 +02:00 (CEST) |
| Date last edited |
2021-04-22 08:28:49 +02:00 (CEST) |
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