Dyschromatosis universalis
General Information (adopted from Orphanet):
| Synonyms, Signs: |
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| Number of Symptoms | 0 |
| OrphanetNr: | 241 |
| OMIM Id: |
127500
612715 615402 |
| ICD-10: |
L81.8 |
| UMLs: |
C1306229 |
| MeSH: |
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| MedDRA: |
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| Snomed: |
239082002 |
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
|
| Age of onset: |
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Disease classification (adopted from Orphanet):
| Parent Diseases: |
Genetic hyperpigmentation of the skin
-Rare genetic disease Hyperpigmentation of the skin -Rare skin disease |
Comment:
| This term does not characterize a disease but a group of diseases. Annotations can be found at a more specific level. |
Symptom Information:
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|