Lymphadenopathy
Symptom Information:
Symptom ID: | HPO:0002716 | ||||||||||||||||||||||||||||||||||||||||||
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 the immune system(HPO:0002715) Abnormality of the lymphatic system(HPO:0100763) Abnormality of the lymph nodes(HPO:0002733) Lymphadenopathy(HPO:0002716) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641) Lymphatic system disorders NEC(MedDRA:10025198) Lymphadenopathy(HPO:0002716) |
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Database Frequency: | 129 / 7739 | ||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III | (OMIM:615559) |
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V | (OMIM:616100) |
Acquired hypertrichosis lanuginosa | (Orphanet:2221) |
Adamantinoma | (Orphanet:55881) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Alpha heavy-chain disease | (Orphanet:100025) |
Alström syndrome | (Orphanet:64) |
Apolipoprotein A-I deficiency | (Orphanet:425) |
Autoimmune lymphoproliferative syndrome with recurrent infections | (Orphanet:275517) |
Autosomal recessive lymphoproliferative disease | (Orphanet:238505) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
Behçet disease | (Orphanet:117) |
Blau syndrome | (Orphanet:90340) |
CINCA syndrome | (Orphanet:1451) |
Carcinoma of the gallbladder | (Orphanet:56044) |
Carney triad | (Orphanet:139411) |
Castleman disease | (Orphanet:160) |
Choreoacanthocytosis | (Orphanet:2388) |
Chédiak-Higashi syndrome | (Orphanet:167) |
Classical mycosis fungoides | (Orphanet:2584) |
Cogan syndrome | (Orphanet:1467) |
Cold agglutinin disease | (Orphanet:56425) |
Combined immunodeficiency due to CRAC channel dysfunction | (Orphanet:169090) |
Combined immunodeficiency due to STIM1 deficiency | (Orphanet:317430) |
Common variable immunodeficiency | (Orphanet:1572) |
Congenital toxoplasmosis | (Orphanet:858) |
Cyclic neutropenia | (Orphanet:2686) |
Deafness - lymphedema - leukemia | (Orphanet:3226) |
Desmoplastic small round cell tumor | (Orphanet:83469) |
Drug rash with eosinophilia and systemic symptoms | (Orphanet:139402) |
Eosinophilic granuloma | (Orphanet:99871) |
Esophageal adenocarcinoma | (Orphanet:99976) |
Esophageal carcinoma | (Orphanet:70482) |
Esophageal squamous cell carcinoma | (Orphanet:99977) |
Faisalabad histiocytosis | (Orphanet:254707) |
Familial Mediterranean fever | (Orphanet:342) |
Familial hemophagocytic lymphohistiocytosis | (Orphanet:540) |
Felty syndrome | (Orphanet:47612) |
Fish-eye disease | (Orphanet:79292) |
Follicular lymphoma | (Orphanet:545) |
GOLGI REASSEMBLY STACKING PROTEIN 1 | (OMIM:606867) |
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE | (OMIM:233690) |
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE I | (OMIM:233700) |
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE II | (OMIM:233710) |
GRANULOMATOUS DISEASE, CHRONIC, X-LINKED | (OMIM:306400) |
Gamma heavy-chain disease | (Orphanet:100026) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Granulomatous slack skin | (Orphanet:33111) |
Griscelli disease | (Orphanet:381) |
Griscelli disease type 2 | (Orphanet:79477) |
H syndrome | (Orphanet:168569) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 | (OMIM:267700) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 | (OMIM:603553) |
Hairy cell leukemia variant | (Orphanet:300878) |
Hand-Schüller-Christian disease | (Orphanet:99873) |
Hashimoto-Pritzker syndrome | (Orphanet:99872) |
Hennekam syndrome | (Orphanet:2136) |
Hodgkin lymphoma | (Orphanet:98293) |
Hodgkin lymphoma, classical | (Orphanet:391) |
Hyper-IgM syndrome type 2 | (Orphanet:101089) |
Hyper-IgM syndrome type 5 | (Orphanet:101092) |
Hyperimmunoglobulinemia D with periodic fever | (Orphanet:343) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
IMMUNODEFICIENCY 14 | (OMIM:615513) |
IMMUNODEFICIENCY, COMMON VARIABLE, 1 | (OMIM:607594) |
IMMUNODEFICIENCY, COMMON VARIABLE, 2 | (OMIM:240500) |
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY | (OMIM:614700) |
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | (Orphanet:37042) |
Immunodeficiency due to CD25 deficiency | (Orphanet:169100) |
Immunodeficiency with natural-killer cell deficiency | (Orphanet:75391) |
Kawasaki disease | (Orphanet:2331) |
Kerion celsi | (Orphanet:499) |
Klatskin tumor | (Orphanet:99978) |
LCAT deficiency | (Orphanet:650) |
LIG4 syndrome | (Orphanet:99812) |
LYMPHOPROLIFERATIVE SYNDROME 1 | (OMIM:613011) |
LYMPHOPROLIFERATIVE SYNDROME 2 | (OMIM:615122) |
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1 | (OMIM:308240) |
Lassa fever | (Orphanet:99824) |
Legionellosis | (Orphanet:549) |
Lymphangioleiomyomatosis | (Orphanet:538) |
Lymphoid interstitial pneumonia | (Orphanet:79128) |
Mantle cell lymphoma | (Orphanet:52416) |
Marshall syndrome with periodic fever | (Orphanet:42642) |
Mast cell sarcoma | (Orphanet:66661) |
Melkersson-Rosenthal syndrome | (Orphanet:2483) |
Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency | (Orphanet:319600) |
Mevalonic aciduria | (Orphanet:29) |
Mixed connective tissue disease | (Orphanet:809) |
Mu heavy-chain disease | (Orphanet:100024) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Nephroblastoma | (Orphanet:654) |
Niemann-Pick disease type A | (Orphanet:77292) |
Nodular lymphocyte predominant Hodgkin lymphoma | (Orphanet:86893) |
Omenn syndrome | (Orphanet:39041) |
Osteopetrosis | (Orphanet:2781) |
POEMS syndrome | (Orphanet:2905) |
POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY | (OMIM:615895) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Persistent polyclonal B-cell lymphocytosis | (Orphanet:300324) |
Pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome | (Orphanet:254723) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Polyglucosan body myopathy type 1 | (ORPHA:397937) |
Primary cutaneous anaplastic large cell lymphoma | (Orphanet:300865) |
Primary cutaneous lymphoma | (Orphanet:542) |
Pseudomyxoma peritonei | (Orphanet:26790) |
Pulmonary capillary hemangiomatosis | (Orphanet:199241) |
Pulmonary venoocclusive disease | (Orphanet:31837) |
Pyogenic arthritis - pyoderma gangrenosum - acne | (Orphanet:69126) |
RETICULOENDOTHELIOSIS, X-LINKED | (OMIM:312500) |
Reticular dysgenesis | (Orphanet:33355) |
Rhabdoid tumor | (Orphanet:69077) |
Roifman syndrome | (Orphanet:353298) |
Rosaï-Dorfman disease | (Orphanet:158014) |
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION | (OMIM:607944) |
Sarcoidosis | (Orphanet:797) |
Schnitzler syndrome | (Orphanet:37748) |
Scrub typhus | (Orphanet:83317) |
Systemic mastocytosis | (Orphanet:2467) |
Sézary syndrome | (Orphanet:3162) |
T-B+ severe combined immunodeficiency due to CD45 deficiency | (Orphanet:169157) |
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency | (Orphanet:169154) |
T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY | (OMIM:615387) |
Thymoma | (Orphanet:99867) |
Waldenström macroglobulinemia | (Orphanet:33226) |
X-linked lymphoproliferative disease | (Orphanet:2442) |