Primary cutaneous anaplastic large cell lymphoma
General Information (adopted from Orphanet):
Synonyms, Signs: |
C-ALCL |
Number of Symptoms | 9 |
OrphanetNr: | 300865 |
OMIM Id: |
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ICD-10: |
C86.6 |
UMLs: |
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MeSH: |
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MedDRA: |
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Snomed: |
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Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
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Age of onset: |
Childhood Adolescent Adult [Orphanet] |
Disease classification (adopted from Orphanet):
Parent Diseases: |
Primary cutaneous CD30+ T-cell lymphoproliferative disease
-Rare hematologic disease -Rare oncologic disease -Rare skin disease |
Symptom Information:
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(HPO:0001357) | Plagiocephaly | Occasional [Orphanet] | 106 / 7739 | |||
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(HPO:0004325) | Decreased body weight | Occasional [Orphanet] | 492 / 7739 | |||
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(HPO:0000989) | Pruritus | Very frequent [Orphanet] | 111 / 7739 | |||
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(HPO:0001031) | Subcutaneous lipoma | Frequent [Orphanet] | 112 / 7739 | |||
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(HPO:0200042) | Skin ulcer | Very frequent [Orphanet] | 138 / 7739 | |||
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(HPO:0002665) | Lymphoma | Very frequent [Orphanet] | 60 / 7739 | |||
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(HPO:0002716) | Lymphadenopathy | Frequent [Orphanet] | 129 / 7739 | |||
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(HPO:0001324) | Muscle weakness | Occasional [Orphanet] | 859 / 7739 | |||
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(HPO:0030350) | Erythematous papule | Very frequent [Orphanet] | 123 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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