Generalized lymphadenopathy

Symptom Information:

Symptom ID: HPO:0008940
Synonyms:
Lymphadenopathy [Orphanet:36150]
Lymphadenopathy (disorder) [Orphanet:36150]
Generalized lymphadenopathy [OMIM:Generalized 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:0002716 "Lymphadenopathy" [Orphanet:36150]
Orphanet:36150 "Lymphadenopathy/polyadenopathies" [Orphanet:36150]
OMIM: "Generalized lymphadenopathy" [OMIM:Generalized 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" [Orphanet:36150]
Is a (Direct Parents):
HPO         Lymphadenopathy
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)
                   Generalized lymphadenopathy(HPO:0008940)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641)
       Lymphatic system disorders NEC(MedDRA:10025198)
          Generalized lymphadenopathy(HPO:0008940)
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

Faisalabad histiocytosis (Orphanet:254707)
Fish-eye disease (Orphanet:79292)
H syndrome (Orphanet:168569)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome (Orphanet:37042)
LCAT deficiency (Orphanet:650)
Lymphangioleiomyomatosis (Orphanet:538)
Niemann-Pick disease type A (Orphanet:77292)
Persistent polyclonal B-cell lymphocytosis (Orphanet:300324)
Pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome (Orphanet:254723)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Rosaï-Dorfman disease (Orphanet:158014)
SARCOIDOSIS, SUSCEPTIBILITY TO, 1 (OMIM:181000)
Sarcoidosis (Orphanet:797)