Lymphoma
Symptom Information:
Symptom ID: | HPO:0002665 | ||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of blood and blood-forming tissues(HPO:0001871) Hematological neoplasm(HPO:0004377) Lymphoma(HPO:0002665) Neoplasm(HPO:0002664) Neoplasm by anatomical site(HPO:0011793) 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) |
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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) |