Hodgkin lymphoma, classical

General Information (adopted from Orphanet):

Synonyms, Signs: Classical Hodgkin disease
Classical Hodgkin&#39
s disease
Classical Hodgkin&#39
s lymphoma
Number of Symptoms 27
OrphanetNr: 391
OMIM Id: 236000
300221
400021
ICD-10: C81
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Unknown
[Orphanet]
Age of onset: All ages
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Hodgkin lymphoma
 -Rare hematologic disease
 -Rare oncologic disease

Symptom Information: Sort by abundance 

1
 (HPO:0001357) Plagiocephaly Frequent [Orphanet] 106 / 7739
2
 (HPO:0002066) Gait ataxia Occasional [Orphanet] 327 / 7739
3
 (HPO:0002315) Headache Occasional [Orphanet] 175 / 7739
4
 (HPO:0009830) Peripheral neuropathy Occasional [Orphanet] 206 / 7739
5
 (HPO:0002653) Bone pain Occasional [Orphanet] 75 / 7739
6
 (HPO:0002797) Osteolysis Occasional [Orphanet] 68 / 7739
7
 (HPO:0100749) Chest pain Frequent [Orphanet] 92 / 7739
8
 (HPO:0002039) Anorexia Frequent [Orphanet] 62 / 7739
9
 (HPO:0001744) Splenomegaly Occasional [Orphanet] 337 / 7739
10
 (HPO:0002240) Hepatomegaly Occasional [Orphanet] 467 / 7739
11
 (HPO:0004325) Decreased body weight Frequent [Orphanet] 492 / 7739
12
 (HPO:0000989) Pruritus Frequent [Orphanet] 111 / 7739
13
 (HPO:0000988) Skin rash Occasional [Orphanet] 98 / 7739
14
 (HPO:0003459) Polyclonal elevation of IgM 4 / 7739
15
 (HPO:0001876) Pancytopenia Occasional [Orphanet] 89 / 7739
16
 (HPO:0003347) Impaired lymphocyte transformation with phytohemagglutinin 6 / 7739
17
 (HPO:0002665) Lymphoma Very frequent [Orphanet] 60 / 7739
18
 (HPO:0012189) Hodgkin lymphoma 5 / 7739
19
 (HPO:0001945) Fever Frequent [Orphanet] 218 / 7739
20
 (HPO:0002105) Hemoptysis Occasional [Orphanet] 30 / 7739
21
 (HPO:0002093) Respiratory insufficiency Occasional [Orphanet] 410 / 7739
22
 (HPO:0002664) Neoplasm Occasional [Orphanet] 111 / 7739
23
 (HPO:0010978) Abnormality of immune system physiology Very frequent [Orphanet] 148 / 7739
24
 (HPO:0002716) Lymphadenopathy Very frequent [Orphanet] 129 / 7739
25
 (HPO:0001324) Muscle weakness Very frequent [Orphanet] 859 / 7739
26
 (HPO:0000007) Autosomal recessive inheritance 2538 / 7739
27
 ([DEL]MedDRA:10011224) Cough Frequent [Orphanet] 70 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: