Phenotype #0000026927
| Individual ID |
00033498 |
| Associated disease |
LCA |
| Phenotype details |
Bone specule like changes; Bull's eye appearence; Atrophic macular lesions; drusion like deposits; Oculodigital Phenomena; Onset Visual Loss, Severe pigmentary retinopathy, Atrophy of retinal pigment, mottling of hypopigmentation. |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal recessive |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Raheel Qamar |
| Database submission license |
No license selected |
| Created by |
Raheel Qamar |
| Date created |
2012-10-12 13:26:32 +02:00 (CEST) |
| Date last edited |
N/A |
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