Lymphadenopathy

Symptom Information:

Symptom ID: HPO:0002716
Synonyms:
Lymph node hyperplasia [HPO:0002716]
Lymphadenopathy (disorder) [Orphanet:36150]
Lymphadenopathy [Orphanet:36150]
Lymph node hyperplasia [OMIM:Lymph node hyperplasia]
Lymphadenopathy [OMIM:Lymphadenopathy]
Lymphadenopathy/polyadenopathies [Orphanet:36150]
Lymphadenopathy [MedDRA:10025197]
Adenopathy [MedDRA:10025197]
Axillary adenopathy [MedDRA:10025197]
Axillary lymph nodes enlarged [MedDRA:10025197]
Enlarged lymph nodes (excl infective) [MedDRA:10025197]
Enlargement of lymph nodes [MedDRA:10025197]
Gland in neck [MedDRA:10025197]
Glands swollen [MedDRA:10025197]
Groin nodes [MedDRA:10025197]
Lymph nodes cervical swollen [MedDRA:10025197]
Lymph nodes enlarged [MedDRA:10025197]
Lymph nodes, enlarged (excl lymphadenitis) [MedDRA:10025197]
Lymphadenopathy cervical [MedDRA:10025197]
Lymphadenopathy inguinal [MedDRA:10025197]
Lymphadenopathy massive [MedDRA:10025197]
Lymphadenopathy thoracic [MedDRA:10025197]
Lymphadenosis [MedDRA:10025197]
Mucocutaneous lymph node [MedDRA:10025197]
Swollen glands [MedDRA:10025197]
Lymphadenopathy axillary [MedDRA:10025197]
Lymph node disorder [MedDRA:10025197]
Occipital lymphadenopathy [MedDRA:10025197]
Lymphoid nodule [MedDRA:10025197]
Submandibular lymphadenopathy [MedDRA:10025197]
Adenomegaly [MedDRA:10025197]
Swollen lymph nodes [MedDRA:10025197]
Generalised lymphadenopathy [MedDRA:10025197]
Generalized lymphadenopathy [MedDRA:10025197]
Regional lymphadenopathy [MedDRA:10025197]
Fluctuant lymph nodes [MedDRA:10025197]
Peripheral lymphadenopathy [MedDRA:10025197]
Cervical lymphadenopathy [OMIM:Cervical lymphadenopathy]
Enlarged lymph nodes [OMIM:Enlarged lymph nodes]
Lymphadenopathy (cervical, inguinal, axillary) [OMIM:Lymphadenopathy (cervical, inguinal, axillary)]
Lymphadenopathy, generalized (in some patients) [OMIM:Lymphadenopathy, generalized (in some patients)]
Submandibular lymphadenopathy [OMIM:Submandibular lymphadenopathy]
Quality:
Cross references:
HPO:0008940 "Generalized lymphadenopathy" [Orphanet:36150]
Orphanet:36150 "Lymphadenopathy/polyadenopathies" [Orphanet:36150]
OMIM: "Lymph node hyperplasia" [OMIM:Lymph node hyperplasia]
OMIM: "Lymphadenopathy" [OMIM:Lymphadenopathy]
OMIM: "Cervical lymphadenopathy" [OMIM:Cervical lymphadenopathy]
OMIM: "Enlarged lymph nodes" [OMIM:Enlarged lymph nodes]
OMIM: "Lymphadenopathy (cervical, inguinal, axillary)" [OMIM:Lymphadenopathy (cervical, inguinal, axillary)]
OMIM: "Lymphadenopathy, generalized (in some patients)" [OMIM:Lymphadenopathy, generalized (in some patients)]
OMIM: "Submandibular lymphadenopathy" [OMIM:Submandibular lymphadenopathy]
UMLS:C0497156 "Lymphadenopathy" [HPO:0002716]
UMLS:C0497156 "Lymphadenopathy" [Orphanet:36150]
Is a (Direct Parents):
HPO         Abnormality of the lymph nodes
Orphanet Abnormality of the lymphatic system
MedDRA Lymphatic system disorders NEC
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)
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)