purpura, thrombotic thrombocytopenic

Preferred Label : purpura, thrombotic thrombocytopenic;

MeSH definition : An acquired, congenital, or familial disorder caused by PLATELET AGGREGATION with THROMBOSIS in terminal arterioles and capillaries. Clinical features include THROMBOCYTOPENIA; HEMOLYTIC ANEMIA; AZOTEMIA; FEVER; and thrombotic microangiopathy. The classical form also includes neurological symptoms and end-organ damage, such as RENAL FAILURE.; An acquired, congenital, or familial disorder caused by PLATELET AGGREGATION with THROMBOSIS in terminal arterioles and capillaries. Clinical features include THROMBOCYTOPENIA; HEMOLYTIC ANEMIA; AZOTEMIA; FEVER; and thrombotic microangiopathy. The classical form also includes neurological symptoms and end-organ damage, such as RENAL FAILURE. Mutations in the ADAMTS13 PROTEIN gene have been identified in familial cases.;

MeSH synonym : purpura, thrombotic thrombopenic; thrombopenic purpura, thrombotic; thrombotic thrombopenic purpura; moschcowitz disease; thrombotic thrombocytopenic purpura; moschkowitz disease; thrombocytopenic purpura, thrombotic;

CISMeF synonym : anemia, microangiopathic hemolytic; anemias, microangiopathic hemolytic; hemolytic anemia, microangiopathic; hemolytic anemias, microangiopathic; microangiopathic hemolytic anemias; familial thrombotic microangiopathies; microangiopathies, familial thrombotic; purpuras, thrombotic thrombocytopenic; purpuras, thrombotic thrombopenic; thrombocytopenic purpuras, thrombotic; thrombopenic purpuras, thrombotic; thrombotic microangiopathies, familial; thrombotic thrombocytopenic purpuras; thrombotic thrombopenic purpuras; disease, moschcowitz; disease, moschkowitz; syndrome, Schulman-Upshaw; syndrome, Upshaw-Schulman;

MeSH hyponym : familial thrombotic thrombocytopenic purpura; congenital thrombotic thrombocytopenic purpura; Schulman-Upshaw Syndrome; Schulman Upshaw Syndrome; Upshaw-Schulman Syndrome; Upshaw Schulman Syndrome; Thrombotic Thrombocytopenic Purpura, Congenital; Upshaw Factor, Deficiency of; Microangiopathic Hemolytic Anemia, Congenital; Thrombotic Microangiopathy, Familial; Familial Thrombotic Microangiopathy; Microangiopathy, Familial Thrombotic; Thrombotic Thrombocytopenic Purpura, Familial; Familial Thrombotic Thrombocytopenia Purpura;

Wikipedia link : https://en.wikipedia.org/wiki/Thrombotic thrombocytopenic purpura;

Details

Origin ID

D011697;

UMLS CUI

C0034155;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Congenital Thrombotic Thrombocytopenic Purpura [NCIt concept]
- Congenital thrombotic thrombocytopenic purpura [ORDO Disease]
- Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency [ICD-11 More detail]
- Mean Absorption Time [NCIt concept]
- Microangiopathic haemolytic anaemia [MedDRA Preferred Term]
- Microangiopathic hemolytic anemia [HPO term]
- Microangiopathic hemolytic anemia [MedDRA LLT]
- Microangiopathic hemolytic anemia (disorder) [SNOMED CT concept]
- Moschcowitz syndrome [MedDRA LLT]
- Multifocal atrial tachycardia [ORDO Disease]
- Multinational Association of Supportive Care in Cancer Antiemesis Tool [NCIt concept]
- Other nonautoimmune hemolytic anemias [ICD-10 Sub-category]
- PURPURA THROMBOPENIC THROMBOTIC [WHO-ART Preferred Term]
- Partial Thromboplastin Time [NCIt concept]
- Protein Tyrosine Phosphatase [NCIt concept]
- Purpura thrombopaenic thrombotic [MedDRA LLT]
- Purpura thrombopenic thrombotic [MedDRA LLT]
- Thrombotic Microangiopathy, CTCAE [NCIt concept]
- Thrombotic Thrombocytopenic Purpura, CTCAE [NCIt concept]
- Thrombotic thrombocytopenic purpura, hereditary [OMIM Phenotype]
- Upshaw-Schulman syndrome (disorder) [SNOMED CT concept]
- hospitals, maternity [CISMeF resources Type]
- microangiopathic hemolytic anemia [SNOMED Notion]
- teaching material [CISMeF resources Type]
- thrombotic thrombocytopenic purpura [Blood Transfusion thesaurus concept]
Currated CISMeF NLP mapping
- Thrombocytopenic purpura, thrombotic [MedDRA LLT]
- Thrombotic Microangiopathy [NCIt concept]
- Thrombotic Thrombocytopenic Purpura [NCIt concept]
- Thrombotic microangiopathy [ICD-10 Sub-category]
- Thrombotic microangiopathy [ICD-10 Sub-category (who)]
- Thrombotic microangiopathy [MedDRA Preferred Term]
- Thrombotic microangiopathy [TUV Concept]
- Thrombotic microangiopathy [TUV Term]
- Thrombotic microangiopathy [ICD-9 code]
- Thrombotic microangiopathy [ORDO Disease]
- Thrombotic microangiopathy (disorder) [SNOMED CT concept]
- Thrombotic microangiopathy NOS [MedDRA LLT]
- Thrombotic thrombocytopenic purpura [PASCAL descriptor]
- Thrombotic thrombocytopenic purpura [ICD-11 Sub-sub category]
- Thrombotic thrombocytopenic purpura [MedDRA Preferred Term]
- Thrombotic thrombocytopenic purpura [ORDO Disease]
- Thrombotic thrombocytopenic purpura (disorder) [SNOMED CT concept]
- thrombotic microangiopathy [COVID-19 Thesaurus concept]
- thrombotic microangiopathy [Blood Transfusion thesaurus concept]
- thrombotic thrombocytopenic purpura [DO Concept]
- thrombotic thrombocytopenic purpura [Disease (Nov.)]
- thrombotic thrombocytopenic purpura [SNOMED Notion]
DO Cross reference
- thrombotic thrombocytopenic purpura [DO Concept]
Indexing information
- platelet agglutinating protein, thrombotic thrombocytopenic purpura [MeSH Supplementary Concept]
Manual BTNT mappings - CISMeF
- Atypical hemolytic uremic syndrome [ORDO Disease]
- Immune-mediated thrombotic thrombocytopenic purpura [ORDO Disease]
- Methylcobalamin deficiency type cblG [ORDO Disease]
- Shiga toxin-associated hemolytic uremic syndrome [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Genetic thrombotic microangiopathy [ORDO Disease]
- Rare renal disease [ORDO Disease]
ORDO relation(s)
- Thrombotic thrombocytopenic purpura [ORDO Disease]
Record concept(s)
- congenital thrombotic thrombocytopenic purpura [MeSH concept]
- familial thrombotic thrombocytopenic purpura [MeSH concept]
- purpura, thrombotic thrombocytopenic [MeSH concept]
Related MeSH Supplementary Concept(s)
- thrombotic thrombocytopenic purpura, acquired [MeSH Supplementary Concept]
See also inter- (CISMeF)
- Drug induced thrombotic thrombocytopenic purpura (disorder) [SNOMED CT concept]
- microangiopathic hemolytic anemia [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Moschcowitz syndrome [MedDRA LLT]
- PURPURA THROMBOPENIC THROMBOTIC [WHO-ART Preferred Term]
- Purpura thrombopaenic thrombotic [MedDRA LLT]
- Purpura thrombopenic thrombotic [MedDRA LLT]
- Thrombocytopenic purpura, thrombotic [MedDRA LLT]
- Thrombotic Thrombocytopenic Purpura [NCIt concept]
- Thrombotic thrombocytopenic purpura [MedDRA Preferred Term]
- Thrombotic thrombocytopenic purpura [ORDO Disease]
- Thrombotic thrombocytopenic purpura [PASCAL descriptor]
- Thrombotic thrombocytopenic purpura (disorder) [SNOMED CT concept]
- thrombotic thrombocytopenic purpura [DO Concept]
- thrombotic thrombocytopenic purpura [Disease (Nov.)]
- thrombotic thrombocytopenic purpura [SNOMED Notion]

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