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1187615007: Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4674359014 Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4674360016 TAFRO syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4674361017 TAFRO (thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4674362012 Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5399656016 A rare systemic disease characterized by acute or subacute onset of thrombocytopenia, anasarca (edema, pleural effusion, ascites), and systemic inflammation (fever and/or elevated C-reactive protein). Minor diagnostic categories are Castleman's disease-like features on lymph node biopsy, reticulin myelofibrosis and/or increased number of megakaryocytes in bone marrow, progressive renal insufficiency, and mild organomegaly including hepatosplenomegaly and lymphadenopathy. Most patients show elevated levels of serum alkaline phosphatase, while marked polyclonal hypergammopathy is rare. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399657013 A rare systemic disease characterised by acute or subacute onset of thrombocytopenia, anasarca (oedema, pleural effusion, ascites), and systemic inflammation (fever and/or elevated C-reactive protein). Minor diagnostic categories are Castleman's disease-like features on lymph node biopsy, reticulin myelofibrosis and/or increased number of megakaryocytes in bone marrow, progressive renal insufficiency, and mild organomegaly including hepatosplenomegaly and lymphadenopathy. Most patients show elevated levels of serum alkaline phosphatase, while marked polyclonal hypergammopathy is rare. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4674359014 Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4674360016 TAFRO syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4674361017 TAFRO (thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4674362012 Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4674363019 A rare systemic disease characterized by acute or subacute onset of thrombocytopenia, anasarca (edema, pleural effusion, ascites) and systemic inflammation (fever and/or elevated C-reactive protein). Minor diagnostic categories are Castleman disease-like features on lymph node biopsy, reticulin myelofibrosis and/or increased number of megakaryocytes in bone marrow, progressive renal insufficiency and mild organomegaly including hepatosplenomegaly and lymphadenopathy. Most patients show elevated levels of serum alkaline phosphatase while marked polyclonal hypergammopathy is rare. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4674364013 A rare systemic disease characterised by acute or subacute onset of thrombocytopenia, anasarca (oedema, pleural effusion, ascites) and systemic inflammation (fever and/or elevated C-reactive protein). Minor diagnostic categories are Castleman disease-like features on lymph node biopsy, reticulin myelofibrosis and/or increased number of megakaryocytes in bone marrow, progressive renal insufficiency and mild organomegaly including hepatosplenomegaly and lymphadenopathy. Most patients show elevated levels of serum alkaline phosphatase while marked polyclonal hypergammopathy is rare. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399656016 A rare systemic disease characterized by acute or subacute onset of thrombocytopenia, anasarca (edema, pleural effusion, ascites), and systemic inflammation (fever and/or elevated C-reactive protein). Minor diagnostic categories are Castleman's disease-like features on lymph node biopsy, reticulin myelofibrosis and/or increased number of megakaryocytes in bone marrow, progressive renal insufficiency, and mild organomegaly including hepatosplenomegaly and lymphadenopathy. Most patients show elevated levels of serum alkaline phosphatase, while marked polyclonal hypergammopathy is rare. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399657013 A rare systemic disease characterised by acute or subacute onset of thrombocytopenia, anasarca (oedema, pleural effusion, ascites), and systemic inflammation (fever and/or elevated C-reactive protein). Minor diagnostic categories are Castleman's disease-like features on lymph node biopsy, reticulin myelofibrosis and/or increased number of megakaryocytes in bone marrow, progressive renal insufficiency, and mild organomegaly including hepatosplenomegaly and lymphadenopathy. Most patients show elevated levels of serum alkaline phosphatase, while marked polyclonal hypergammopathy is rare. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3436211001000110 TAFRO-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3436211001000110 TAFRO-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Is a Disorder characterized by edema true Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Is a Inflammatory disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Is a Thrombocytopenic disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Is a Fever (finding) true Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Is a Anasarca true Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Is a Systemic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Associated morphology Anasarca true Inferred relationship Existential restriction modifier (core metadata concept) 3
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Interprets Hemostatic function true Inferred relationship Existential restriction modifier (core metadata concept) 1
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 1
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Interprets Platelet count true Inferred relationship Existential restriction modifier (core metadata concept) 2
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Interprets Body temperature (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 5
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Has interpretation Above reference range true Inferred relationship Existential restriction modifier (core metadata concept) 5
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Is a Febrile disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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