Granulomatous slack skin
General Information (adopted from Orphanet):
| Synonyms, Signs: |
|
| Number of Symptoms | 6 |
| OrphanetNr: | 33111 |
| OMIM Id: |
|
| ICD-10: |
C84.0 |
| UMLs: |
C0376407 C0457002 |
| MeSH: |
|
| MedDRA: |
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| Snomed: |
277796003 |
Prevalence, inheritance and age of onset:
| Prevalence: | < 50 cases [Orphanet] |
| Inheritance: |
Not applicable [Orphanet] |
| Age of onset: |
Adult [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Mycosis fungoides and variants
-Rare hematologic disease -Rare oncologic disease -Rare skin disease Rare skin tumor or hamartoma -Rare oncologic disease -Rare skin disease |
Symptom Information:
|
|
(HPO:0001744) | Splenomegaly | Occasional [Orphanet] | 337 / 7739 | |||
|
|
(HPO:0000974) | Hyperextensible skin | Very frequent [Orphanet] | 59 / 7739 | |||
|
|
(HPO:0010783) | Erythema | Very frequent [Orphanet] | 138 / 7739 | |||
|
|
(HPO:0002665) | Lymphoma | Very frequent [Orphanet] | 60 / 7739 | |||
|
|
(HPO:0004332) | Abnormality of lymphocytes | Frequent [Orphanet] | 12 / 7739 | |||
|
|
(HPO:0002716) | Lymphadenopathy | Occasional [Orphanet] | 129 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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