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414629003: Lymphoproliferative disorder (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2530829017 Lymphoproliferative disorder (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2534293012 Lymphoproliferative disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2530829017 Lymphoproliferative disorder (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2530829017 Lymphoproliferative disorder (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2534293012 Lymphoproliferative disorder en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2534293012 Lymphoproliferative disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

202 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lymphoproliferative disorder Is a Proliferation of hematopoietic cell type (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Lymphoid neoplasm Is a True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept)
Immunoproliferative morphology Is a True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept)
Lymphoproliferative disorder following transplantation Associated morphology False Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept)
Lymphoproliferative disorder Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
Histiocytic necrotizing lymphadenitis Associated morphology False Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept)
Reactive follicular hyperplasia in the elderly Associated morphology False Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 2
Post-transplantation lymphoproliferative syndrome Associated morphology False Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept)
Virus-associated atypical lymphoproliferative disorder (disorder) Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 2
Atypical lymphoproliferative disorder Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
Rosai-Dorfman disease Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 2
Lymphoid interstitial pneumonitis (disorder) Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked lymphoproliferative syndrome Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
Hemophagocytic lymphohistiocytosis due to infection (disorder) Associated morphology False Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 5
Familial hemophagocytic lymphohistiocytosis Associated morphology False Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 4
Primary cutaneous CD30+ T-cell lymphoproliferative disorder Is a True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept)
Monomorphic posttransplant lymphoproliferative disorder (disorder) Associated morphology False Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept)
infection au VIH causant une pneumopathie lymphoïde interstitielle Associated morphology False Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept)
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
Lymphoproliferative disorder after transplantation of bone marrow Associated morphology False Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
Dianzani autoimmune lymphoproliferative disease (DALD) is a very rare disorder characterized by autoimmunity, lymphadenopathy and/or splenomegaly. Associated morphology False Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept)
Dianzani autoimmune lymphoproliferative disease (DALD) is a very rare disorder characterized by autoimmunity, lymphadenopathy and/or splenomegaly. Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
Natural killer cell enteropathy (disorder) Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
RAS-associated autoimmune leukoproliferative disease (disorder) Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 4
Chronic cold agglutinin disease associated with B-cell neoplasm (disorder) Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 8
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
Persistent polyclonal B-cell lymphocytosis (PPBL) is a rare, generally benign, lymphoproliferative hematological disease characterized by chronic, stable, persistent, polyclonal lymphocytosis of memory B-cell origin, the presence of binucleated lymphocytes in the peripheral blood, and a polyclonal increase in serum immunoglobulin M (IgM). Patients are most frequently asymptomatic or may present with mild splenomegaly. Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 2
Acquired angioedema due to activation of the classical complement pathway related to an underlying lymphoreticular disorder particularly lymphoma or monoclonal gammopathy of unknown significance (MGUS) Associated morphology False Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
Lymphoproliferative disorder caused by methotrexate Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive lymphoproliferative disease (disorder) Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
Histiocytic necrotizing lymphadenitis Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 2
Iatrogenic immunodeficiency-associated lymphoproliferative disorder (disorder) Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
Germinotropic lymphoproliferative disorder caused by Human herpesvirus 8 Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
Hydroa vacciniforme-like lymphoproliferative disorder Is a True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept)
Autoimmune lymphoproliferative syndrome Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked lymphoproliferative disease due to SH2D1A deficiency (disorder) Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked lymphoproliferative disease due to XIAP deficiency Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare immune dysregulation disease with immunodeficiency characterised by infantile or childhood onset of a variable phenotype including recurrent/persistent bacterial, fungal, and viral infections with involvement of the skin, lower respiratory tract, and gastrointestinal tract, eczema, allergies, and inflammatory bowel disease, among others. EBV-related smooth muscle tumours have also been reported. Immunophenotyping shows decreased Treg counts, as well as a deficient CD3/CD28 co-stimulation response in CD4+ and CD8+ T-cells. Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
Combined immunodeficiency due to interleukin-2 inducible T cell kinase deficiency (disorder) Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare autosomal recessive primary immunodeficiency characterized by susceptibility to Epstein-Barr virus (EBV)-related disorders (B-cell lymphoproliferative disorders including Hodgkin lymphoma) as well as dysgammaglobulinemia and recurrent infections. Patients can present with recurrent fever, lymphadenopathy, hepatosplenomegaly, Behçet-like stomatitis, pharyngitis, tonsillitis, adenitis, and viral encephalitis. Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare, primary immunodeficiency characterized by variable combination of enteropathy, hypogammaglobulinemia, recurrent respiratory infections, granulomatous lymphocytic interstitial lung disease, lymphocytic infiltration of non-lymphoid organs (intestine, lung, brain, bone marrow, kidney), autoimmune thrombocytopenia or neutropenia, autoimmune hemolytic anemia and lymphadenopathy. Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
STAT3-related early-onset multisystem autoimmune disease Associated morphology True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
Post-transplantation lymphoproliferation (morphologic abnormality) Is a True Lymphoproliferative disorder Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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