Phenotype #0000204094
| Individual ID |
00266318 |
| Associated disease |
USH1 |
| Phenotype details |
Congenital sensorineural hearing impairment (HP:0008527), Myopia (HP:0000545), Nyctalopia (HP:0000662), Rod cone dystrophy (HP:0000510) |
| Diagnosis/Initial |
- |
| Inheritance |
Unknown |
| Diagnosis/Definite |
- |
| Age/Examination |
05y09m (5 years, 9 months) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Omamah Jiman |
| Database submission license |
No license selected |
| Created by |
Omamah Jiman |
| Date created |
2019-10-22 16:15:16 +02:00 (CEST) |
| Date last edited |
2019-10-22 17:27:34 +02:00 (CEST) |
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