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Lymphoid system disorder

MedGen UID:: 9829
•Concept ID:: C0024228
•: Disease or Syndrome

Synonym:	Lymphoid system disease
SNOMED CT:	Disorder of lymphoid system (111590001); Disorders of lymph node and lymphatics (234087005); Disorder of lymphatic system (362971004); Disorder of lymphatics (3305006); Lymphangiopathy (3305006)

Monarch Initiative:	MONDO:0044986

Definition

A disease or disorder that involves the lymphoid system. [from MONDO]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVLymphoid system disorder

Pathological Conditions, Signs and Symptoms
- Pathological process
  - Disease
    - Disorder by Site
      - Hematopoietic and Lymphatic System Disorder
        Lymphoid system disorder
        Acute febrile mucocutaneous lymph node syndrome
        Histiocytosis
        Langerhans cell histiocytosis
        Bone Langerhans Cell Histiocytosis
        Central Nervous System Langerhans Cell Histiocytosis
        Cutaneous Langerhans Cell Histiocytosis
        Eosinophilic granuloma
        Hand-Schuller-Christian disease
        Head and Neck Langerhans Cell Histiocytosis
        Langerhans cell histiocytosis specific to adulthood
        Langerhans cell histiocytosis specific to childhood
        Langerhans Cell Histiocytosis, Disseminated
        Langerhans Cell Histiocytosis, Monostotic
        Langerhans Cell Histiocytosis, Polyostotic
        Recurrent Langerhans Cell Histiocytosis
        Refractory Langerhans Cell Histiocytosis
        Malignant histiocytic disorder
        Follicular dendritic cell sarcoma
        Histiocytic sarcoma
        Interdigitating dendritic cell sarcoma
        Langerhans cell sarcoma
        Mucinous histiocytosis
        Non-Langerhans cell histiocytosis
        Benign cephalic histiocytosis
        Erdheim-Chester disease
        Generalized eruptive histiocytosis
        Hemophagocytic lymphohistiocytosis
        Hereditary progressive mucinous histiocytosis
        Indeterminate dendritic cell tumor
        Juvenile xanthogranuloma
        Multicentric reticulohistiocytosis
        Necrobiotic xanthogranuloma
        Papular xanthoma
        Progressive nodular histiocytosis
        Sea-blue histiocyte syndrome
        Sinus histiocytosis with massive lymphadenopathy
        Sphingomyelin/cholesterol lipidosis
        Xanthoma disseminatum
        Lymphadenitis
        Acute lymphadenitis
        Axillary lymphadenitis
        Cat scratch disease
        cervical lymphadenitis
        Chronic lymphadenitis
        Kikuchi-Fujimoto disease
        Kimura disease
        Mesenteric lymphadenitis
        Postauricular lymphadenitis
        Submandibular adenitis
        Suppurative lymphadenitis
        Lymphadenopathy
        Angioimmunoblastic T-cell lymphoma
        Cutaneous Follicular Helper T-Cell Lymphoma, Angioimmunoblastic-Type
        Follicular Helper T-Cell Lymphoma, Angioimmunoblastic-Type by Ann Arbor Stage
        Recurrent Follicular Helper T-Cell Lymphoma, Angioimmunoblastic-Type
        Refractory Follicular Helper T-Cell Lymphoma, Angioimmunoblastic-Type
        Atypical Lymph Node
        Swollen Lymph Node
        Axillary lymphadenopathy
        Cervical lymphadenopathy
        Chronic noninfectious lymphadenopathy
        Dermatopathic lymphadenitis
        Follicular hyperplasia
        Generalized lymphadenopathy
        Hilar lymph node enlargement
        Inguinal lymphadenopathy
        Localized enlarged lymph nodes
        Lymphadenopathy with Polyclonal Hypergammaglobulinemia
        Paratracheal lymphadenopathy
        Submandibular lymph node enlargement
        Supraclavicular lymphadenopathy
        Lymphangiectasis
        Congenital pulmonary lymphangiectasia
        Intestinal lymphangiectasia
        Primary intestinal lymphangiectasia
        Protein-losing enteropathy
        Secondary intestinal lymphangiectasia
        Pancreatic lymphangiectasis
        Pericardial lymphangiectasia
        Pleural lymphangiectasia
        Pulmonary lymphangiectasia
        Thyroid lymphangiectasia
        Lymphangitis
        Lymphatic malformation
        22q11 Deletion Syndrome
        DiGeorge syndrome
        Lymphedema
        Breast Cancer Lymphedemas
        Chronic acquired lymphedema
        Elephantiasis
        Filarial elephantiasis
        Hereditary lymphedema type I
        Lymphedema of the Head and Neck
        Non-Filarial Lymphedema
        Predominantly lower limb lymphedema
        Lymphocele
        Renal Lymphocele
        Lymphoproliferative disorder
        Agammaglobulinemia
        Activated PI3K-delta syndrome
        Isolated agammaglobulinemia
        AL amyloidosis
        Primary localized amyloidosis
        Primary systemic amyloidosis
        Recurrent AL Amyloidosis
        Recurrent Primary Amyloidosis
        Refractory AL Amyloidosis
        Refractory Primary Amyloidosis
        Alpha-heavy chain disease
        Atypical lymphoproliferative disorder
        Atypical Gastric Lymphoid Hyperplasia
        Castleman disease
        EBV positive mucocutaneous ulcer
        Indolent T-Lymphoblastic Proliferation
        Severe Mosquito Bite Allergy
        Autoimmune lymphoproliferative syndrome
        Autoimmune lymphoproliferative syndrome type 1
        Autoimmune lymphoproliferative syndrome type 4
        Autoimmune lymphoproliferative syndrome type 2A
        Autoimmune lymphoproliferative syndrome type 2B
        Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency
        Autosomal recessive lymphoproliferative disease
        B-Cell Lymphoproliferative Disorder
        B-cell lymphoma
        Follicular Bronchitis/Bronchiolitis
        Nodular lymphocyte predominant Hodgkin lymphoma
        Non-Destructive Post-Transplant Lymphoproliferative Disorder
        Benign Lymphoproliferative Disorder
        Chronic lymphoproliferative disorder of NK-cells
        Infectious mononucleosis
        Lymphocytoma cutis
        Cutaneous Lymphoproliferative Disorder
        Cutaneous Lymphoma
        Cutaneous Mature B-Cell Neoplasm
        Cutaneous Mature T-Cell and NK-Cell Neoplasm
        Cutaneous Precursor Lymphoid Neoplasm
        Dianzani autoimmune lymphoproliferative disease
        Early-onset autoimmunity-autoinflammation-immunodeficiency syndrome
        Epstein-Barr virus-associated malignant lymphoproliferative disorder
        Burkitt lymphoma
        Diffuse large B-cell lymphoma with chronic inflammation
        EBV-positive T-cell lymphoproliferative disorder of childhood
        EBV-Related Lymphoma
        Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly
        Extranodal nasal NK/T cell lymphoma
        HHV8-Positive Germinotropic Lymphoproliferative Disorder
        Hydroa vacciniforme-like lymphoma
        Lymphomatoid granulomatosis
        Plasmablastic lymphoma
        Post-transplant lymphoproliferative disease
        Primary central nervous system lymphoma
        Primary effusion lymphoma
        Systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood
        Familial hyperinflammatory lymphoproliferative immunodeficiency
        Granuloma
        Breast granuloma
        Cholesterol granuloma
        Cutaneous granuloma
        Eosinophilic granulomatosis with polyangiitis
        Foreign body granuloma
        Giant cell granuloma
        Granuloma annulare
        Granuloma by Site
        Granuloma, Respiratory Tract
        Infective granuloma
        Lipogranulomatosis
        Necrotizing granulomatous inflammation
        Non-necrotizing granuloma
        Plasma cell granuloma
        Pyogenic granuloma
        Skin epithelioid hemangioma
        Spermatogenic granuloma
        Suppurative Granuloma
        Hairy cell leukemia
        Progressive Hairy Cell Leukemia Initial Treatment
        Recurrent Hairy Cell Leukemia
        Refractory hairy cell leukemia
        Splenic manifestation of hairy cell leukemia
        Heavy chain disease
        Gamma heavy chain disease (clinical)
        Mu-heavy chain disease
        HHV8-Related Lymphoproliferative Disorder
        Diffuse Large B-Cell Lymphoma Arising in HHV8-Positive Multicentric Castleman Disease
        HHV8-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified
        HHV8-Positive Multicentric Castleman Disease
        Lymphangiomyoma
        Lymphangiomyomatosis
        Lymphoid leukemia
        Acute biphenotypic leukemia
        Acute lymphoid leukemia
        Aggressive NK-cell leukemia
        Aleukemic Lymphoid Leukemia
        B-cell chronic lymphocytic leukemia
        B-Cell Leukemia
        Burkitt Leukemia
        Hairy cell leukemia variant
        Leukemic Phase of Lymphoma
        Plasma cell leukemia
        Precursor Cell Lymphoblastic Leukemia-Lymphoma
        Prolymphocytic leukemia
        T cell chronic lymphocytic lymphoma/leukemia
        T-cell large granular lymphocyte leukemia
        T-cell leukemia
        Lymphoid neoplasm
        Lymphoma
        Neoplastic Post-Transplant Lymphoproliferative Disorder
        Precursor lymphoblastic lymphoma/leukemia
        Recurrent Malignant Lymphoid Neoplasm
        Refractory Malignant Lymphoid Neoplasm
        T-cell and NK-cell neoplasm
        Lymphoproliferative syndrome 1
        Macrophage activation syndrome
        Marek Disease
        Multiple myeloma
        Multiple Myeloma by ISS Stage
        Multiple Myeloma by RISS Stage
        Multiple Myeloma Post-Transplant Lymphoproliferative Disorder
        Non-secretory plasma cell myeloma
        Osteosclerotic plasma cell myeloma
        Recurrent Multiple Myeloma
        Refractory Multiple Myeloma
        Smoldering plasma cell myeloma
        Plasmacytoma
        Anaplastic Plasmacytoma
        Extramedullary plasmacytoma
        Extramedullary soft tissue plasmacytoma
        Primary plasmacytoma of the bone
        Solitary osseous plasmacytoma
        Solitary plasmacytoma of chest wall
        Recurrent Lymphoproliferative Disorder
        Recurrent Lymphomatoid Granulomatosis
        Recurrent Polymorphic Post-Transplant Lymphoproliferative Disorder
        Refractory Lymphoproliferative Disorder
        Refractory Polymorphic Post-Transplant Lymphoproliferative Disorder
        Sarcoidosis
        Cardiac sarcoidosis
        Cerebral sarcoidosis
        Hypercalcemic sarcoidosis
        Pulmonary sarcoidosis
        Skin sarcoidosis
        Uveoparotid fever
        Severe combined immunodeficiency due to CARMIL2 deficiency
        Severe combined immunodeficiency due to CD70 deficiency
        Sezary syndrome
        Recurrent Sezary Syndrome
        Refractory Sezary Syndrome
        STAT3-related early-onset multisystem autoimmune disease
        T/NK-Cell Lymphoproliferative Disorder
        Monomorphic T/NK-Cell Post-Transplant Lymphoproliferative Disorder
        Tumor lysis syndrome
        Waldenstrom macroglobulinemia
        Familial Waldenstrom Macroglobulinemia
        Macroglobulinemia, Waldenstrom, 1
        Macroglobulinemia, Waldenstrom, 2
        Macroglobulinemia, Waldenstrom, somatic
        Recurrent Waldenstrom Macroglobulinemia
        Refractory Waldenstrom Macroglobulinemia
        Smoldering Waldenstrom Macroglobulinemia
        Neoplasm of the thymus
        Benign neoplasm of thymus
        Thymus Lipofibroadenoma
        Thymic carcinoid tumor
        Thymic Neuroendocrine Tumor G1
        Thymic Neuroendocrine Tumor G2
        Thymic epithelial neoplasm
        Combined thymoma
        Thymic carcinoma
        Thymic Epithelial Neoplasm by AJCC v8 Stage
        Thymic neuroendocrine carcinoma
        Thymic Neuroendocrine Neoplasm
        Thymoma
        Thymic neuroendocrine tumor
        Thymus cancer
        Malignant Thymoma
        Metastatic Malignant Neoplasm in the Thymus
        Metastatic Thymic Neuroendocrine Neoplasm
        Thymoliposarcoma
        Thymus lymphoma
        Unresectable Thymic Neuroendocrine Neoplasm
        Thymus Solitary Fibrous Tumor
        Pseudolymphoma
        Cervical Florid Reactive Lymphoid Hyperplasia
        Conjunctival Reactive Lymphoid Hyperplasia
        Reactive lymphoid hyperplasia of lacrimal gland
        Splenic disorder
        Hypersplenism
        Infection of spleen
        Splenic abscess
        Spleen neoplasm
        Benign neoplasm of spleen
        Spleen cancer
        Splenic infarction
        Splenic rupture
        Splenic Rupture Related to Birth
        Splenosis
        Splenic tuberculosis
        Visceral heterotaxy
        Dextrocardia
        Heterotaxy
        Right atrial isomerism
        Situs inversus
        Situs inversus with levocardia
        Wandering spleen
        Thymus hyperplasia

Professional guidelines

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Lymphoid system disorder

Definition

Term Hierarchy

Professional guidelines

PubMed

Recent clinical studies

Etiology

Diagnosis

Therapy

Prognosis

Clinical prediction guides

Recent systematic reviews

Supplemental Content

Table of contents

Clinical resources

Practice guidelines

Consumer resources

Reviews

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