Nodular lymphocyte predominant Hodgkin lymphoma

General Information (adopted from Orphanet):

Synonyms, Signs: NLPHL
Number of Symptoms 13
OrphanetNr: 86893
OMIM Id:
ICD-10: C81.1
UMLs: C1334968
C2239290
MeSH:
MedDRA:
Snomed: 118605002
277608004
70600005

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 Occasional [Orphanet] 106 / 7739
2
 (HPO:0002039) Anorexia Occasional [Orphanet] 62 / 7739
3
 (HPO:0001744) Splenomegaly Occasional [Orphanet] 337 / 7739
4
 (HPO:0002240) Hepatomegaly Occasional [Orphanet] 467 / 7739
5
 (HPO:0004325) Decreased body weight Occasional [Orphanet] 492 / 7739
6
 (HPO:0000989) Pruritus Occasional [Orphanet] 111 / 7739
7
 (HPO:0002665) Lymphoma Very frequent [Orphanet] 60 / 7739
8
 (HPO:0001876) Pancytopenia Occasional [Orphanet] 89 / 7739
9
 (HPO:0001945) Fever Occasional [Orphanet] 218 / 7739
10
 (HPO:0002664) Neoplasm Occasional [Orphanet] 111 / 7739
11
 (HPO:0002716) Lymphadenopathy Very frequent [Orphanet] 129 / 7739
12
 (HPO:0010978) Abnormality of immune system physiology Very frequent [Orphanet] 148 / 7739
13
 (HPO:0001324) Muscle weakness Occasional [Orphanet] 859 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: