Retinal pigmentation
Symptom Information:
| Symptom ID: | MedDRA:10038894 | ||
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HPO:
MedDRA: Eye disorders(MedDRA:10015919) Ocular structural change, deposit and degeneration NEC(MedDRA:10042261) Retinal structural change, deposit and degeneration(MedDRA:10038896) Retinal pigmentation(MedDRA:10038894) |
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| Database Frequency: | 4 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Autosomal recessive chorioretinopathy-microcephaly | (Orphanet:2518) |
| Homocarnosinosis | (Orphanet:2168) |
| Leber congenital amaurosis 16 | (OMIM:614186) |
| Mucopolysaccharidosis type 2 | (Orphanet:580) |