Lymphoma

Symptom Information:

Symptom ID: HPO:0002665
Synonyms:
Malignant lymphoma, no ICD-O subtype (morphologic abnormality) [Orphanet:51020]
Malignant lymphoma (disorder) [Orphanet:51020]
Lymphoma [Orphanet:51020]
Lymphoma [OMIM:Lymphoma]
Lymphoma [MedDRA:10025310]
Gastric lymphoma [MedDRA:10025310]
Gastrointestinal lymphoma [MedDRA:10025310]
Lymphoma malignant [MedDRA:10025310]
Lymphoma NOS [MedDRA:10025310]
Malignant lymphoma [MedDRA:10025310]
Malignant lymphoma NOS [MedDRA:10025310]
Other lymphomas, unspecified site, extranodal and solid organ sites [MedDRA:10025310]
Other malignant lymphomas [MedDRA:10025310]
Other malignant lymphomas involving intra-abdominal lymph nodes [MedDRA:10025310]
Other malignant lymphomas involving intrapelvic lymph nodes [MedDRA:10025310]
Other malignant lymphomas involving intrathoracic lymph nodes [MedDRA:10025310]
Other malignant lymphomas involving lymph nodes of axilla and upper limb [MedDRA:10025310]
Other malignant lymphomas involving lymph nodes of head, face, and neck [MedDRA:10025310]
Other malignant lymphomas involving lymph nodes of inguinal region and lower limb [MedDRA:10025310]
Other malignant lymphomas involving lymph nodes of multiple sites [MedDRA:10025310]
Other malignant lymphomas involving spleen [MedDRA:10025310]
Pulmonary lymphoma [MedDRA:10025310]
Cancer of lymph node [MedDRA:10025310]
Malignant lymphadenopathy [MedDRA:10025310]
Malignant lymphoma of bone [MedDRA:10025310]
Colonic lymphoma [MedDRA:10025310]
Hepatic lymphoma [MedDRA:10025310]
Splenic lymphoma [MedDRA:10025310]
Genital tract lymphoma [MedDRA:10025310]
Lymphoma (in some patients) [OMIM:Lymphoma (in some patients)]
Quality:
Cross references:
HPO:0005526 "Lymphoid leukemia" [Orphanet:51020]
Orphanet:51020 "Lymphoma" [Orphanet:51020]
OMIM: "Lymphoma" [OMIM:Lymphoma]
OMIM: "Lymphoma (in some patients)" [OMIM:Lymphoma (in some patients)]
UMLS:C0024299 "Lymphoma" [HPO:0002665]
UMLS:C0024299 "Lymphoma" [Orphanet:51020]
Is a (Direct Parents):
MedDRA Lymphomas unspecified NEC
HPO         Hematological neoplasm
HPO         Gastric lymphoma
Orphanet Haematological malignancy
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Hematological neoplasm(HPO:0004377)
                Lymphoma(HPO:0002665)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Hematological neoplasm(HPO:0004377)
             Lymphoma(HPO:0002665)
MedDRA:
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Lymphomas NEC(MedDRA:10025323)
       Lymphomas unspecified NEC(MedDRA:10025324)
          Lymphoma(HPO:0002665)
Database Frequency: 60 / 7739
Resource:

All diseases associated with this symptom:

48,XXYY syndrome (Orphanet:10)
Acquired ichthyosis (Orphanet:454)
Acute lymphoblastic leukemia (Orphanet:513)
Aggressive systemic mastocytosis (Orphanet:98850)
Alpha heavy-chain disease (Orphanet:100025)
Autoimmune hemolytic anemia (Orphanet:98375)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal recessive lymphoproliferative disease (Orphanet:238505)
B-CELL LEUKEMIA/LYMPHOMA 3 (OMIM:109560)
Baller-Gerold syndrome (Orphanet:1225)
Bloom syndrome (Orphanet:125)
CARBOXYLESTERASE 1 (OMIM:114835)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
Cartilage-hair hypoplasia (Orphanet:175)
Classical mycosis fungoides (Orphanet:2584)
Common variable immunodeficiency (Orphanet:1572)
Constitutional mismatch repair deficiency syndrome (Orphanet:252202)
Dermatomyositis (Orphanet:221)
Dubowitz syndrome (Orphanet:235)
Dyskeratosis congenita (Orphanet:1775)
EEC syndrome (Orphanet:1896)
Eosinophilic granuloma (Orphanet:99871)
Familial platelet syndrome with predisposition to acute myelogenous leukemia (Orphanet:71290)
Felty syndrome (Orphanet:47612)
Follicular lymphoma (Orphanet:545)
Granulomatous slack skin (Orphanet:33111)
Hashimoto-Pritzker syndrome (Orphanet:99872)
Hodgkin lymphoma (Orphanet:98293)
Hodgkin lymphoma, classical (Orphanet:391)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
IMMUNODEFICIENCY, COMMON VARIABLE, 2 (OMIM:240500)
Isolated punctate palmoplantar keratoderma (Orphanet:2338)
LEUKEMIA/LYMPHOMA, CHRONIC B-CELL, 5 (OMIM:151441)
LIG4 syndrome (Orphanet:99812)
LYMPHOPROLIFERATIVE SYNDROME 2 (OMIM:615122)
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1 (OMIM:308240)
Li-Fraumeni syndrome (Orphanet:524)
Lymphoid hypereosinophilic syndrome (Orphanet:314970)
Mixed-type autoimmune hemolytic anemia (Orphanet:90036)
Nijmegen breakage syndrome (Orphanet:647)
Nodular lymphocyte predominant Hodgkin lymphoma (Orphanet:86893)
Non-Hodgkin lymphoma (Orphanet:547)
Non-polyposis Turcot syndrome (Orphanet:99817)
Omenn syndrome (Orphanet:39041)
Primary cutaneous anaplastic large cell lymphoma (Orphanet:300865)
Primary cutaneous lymphoma (Orphanet:542)
Primary effusion lymphoma (Orphanet:48686)
Primary intestinal lymphangiectasia (Orphanet:90362)
Punctate palmoplantar keratoderma type 1 (Orphanet:79501)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
RAPADILINO syndrome (Orphanet:3021)
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER (OMIM:614470)
Retinoblastoma (Orphanet:790)
Schnitzler syndrome (Orphanet:37748)
Sézary syndrome (Orphanet:3162)
WT limb-blood syndrome (Orphanet:3466)
Waldenström macroglobulinemia (Orphanet:33226)
Wiskott-Aldrich syndrome (Orphanet:906)
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia (Orphanet:317476)
X-linked lymphoproliferative disease (Orphanet:2442)