Hodgkin lymphoma
General Information (adopted from Orphanet):
Synonyms, Signs: |
Hodgkin' s disease Hodgkin' s lymphoma |
Number of Symptoms | 21 |
OrphanetNr: | 98293 |
OMIM Id: |
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ICD-10: |
C81 |
UMLs: |
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MeSH: |
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MedDRA: |
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Snomed: |
14537002 |
Prevalence, inheritance and age of onset:
Prevalence: | 10 of 100 000 [Orphanet] |
Inheritance: |
Multifactorial [Orphanet] |
Age of onset: |
Adult [Orphanet] |
Disease classification (adopted from Orphanet):
Parent Diseases: |
Epstein-Barr virus-associated malignant lymphoproliferative disorder
-Rare oncologic disease Lymphoma -Rare hematologic disease -Rare oncologic disease |
Symptom Information:
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(HPO:0001357) | Plagiocephaly | Frequent [Orphanet] | 106 / 7739 | |||
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(HPO:0009830) | Peripheral neuropathy | Occasional [Orphanet] | 206 / 7739 | |||
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(HPO:0002066) | Gait ataxia | Occasional [Orphanet] | 327 / 7739 | |||
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(HPO:0002315) | Headache | Occasional [Orphanet] | 175 / 7739 | |||
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(HPO:0100749) | Chest pain | Frequent [Orphanet] | 92 / 7739 | |||
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(HPO:0002653) | Bone pain | Occasional [Orphanet] | 75 / 7739 | |||
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(HPO:0002240) | Hepatomegaly | Occasional [Orphanet] | 467 / 7739 | |||
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(HPO:0002039) | Anorexia | Frequent [Orphanet] | 62 / 7739 | |||
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(HPO:0001744) | Splenomegaly | Occasional [Orphanet] | 337 / 7739 | |||
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(HPO:0004325) | Decreased body weight | Frequent [Orphanet] | 492 / 7739 | |||
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(HPO:0000989) | Pruritus | Frequent [Orphanet] | 111 / 7739 | |||
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(HPO:0002665) | Lymphoma | Very frequent [Orphanet] | 60 / 7739 | |||
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(HPO:0001876) | Pancytopenia | Occasional [Orphanet] | 89 / 7739 | |||
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(HPO:0001945) | Fever | Frequent [Orphanet] | 218 / 7739 | |||
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(HPO:0002093) | Respiratory insufficiency | Occasional [Orphanet] | 410 / 7739 | |||
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(HPO:0002105) | Hemoptysis | Occasional [Orphanet] | 30 / 7739 | |||
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(HPO:0002664) | Neoplasm | Occasional [Orphanet] | 111 / 7739 | |||
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(HPO:0002716) | Lymphadenopathy | Very frequent [Orphanet] | 129 / 7739 | |||
|
(HPO:0010978) | Abnormality of immune system physiology | Very frequent [Orphanet] | 148 / 7739 | |||
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(HPO:0001324) | Muscle weakness | Very frequent [Orphanet] | 859 / 7739 | |||
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([DEL]MedDRA:10011224) | Cough | Frequent [Orphanet] | 70 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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