thrombasthenia

Preferred Label : thrombasthenia;

MeSH definition : A congenital bleeding disorder with prolonged bleeding time, absence of aggregation of platelets in response to most agents, especially ADP, and impaired or absent clot retraction. Platelet membranes are deficient in or have a defect in the glycoprotein IIb-IIIa complex (PLATELET GLYCOPROTEIN GPIIB-IIIA COMPLEX).;

MeSH synonym : thrombasthenias; glanzmann thrombasthenia; thrombasthenia, glanzmann; Thrombasthenia of Glanzmann and Naegeli; Glanzmann Thrombasthenia, Type A; Platelet Glycoprotein IIb-IIIa Deficiency; Platelet Glycoprotein IIb IIIa Deficiency; Platelet Fibrinogen Receptor, Deficiency of; Platelet Glycoprotein 2b-3a Deficiency; Platelet Glycoprotein 2b 3a Deficiency; Glycoprotein Complex IIb-IIIa, Deficiency Of; Glycoprotein Complex IIb IIIa, Deficiency Of; GP IIb-IIIa Complex, Deficiency Of; GP IIb IIIa Complex, Deficiency Of; Deficiency of GP 2b 3a Complex;

MeSH hyponym : Glanzmann thrombasthenia, type A; Platelet Fibrinogen Receptor, Deficiency of; Platelet Glycoprotein IIb-IIIa Deficiency; Platelet Glycoprotein IIb IIIa Deficiency; Glycoprotein Complex IIb-IIIa, Deficiency Of; Glycoprotein Complex IIb IIIa, Deficiency Of; GP IIb-IIIa Complex, Deficiency Of; GP IIb IIIa Complex, Deficiency Of; Deficiency of GP 2b 3a Complex; Platelet Glycoprotein 2b-3a Deficiency; Platelet Glycoprotein 2b 3a Deficiency;

Wikipedia link : https://en.wikipedia.org/wiki/Thrombasthenia;

Details

Origin ID

D013915;

UMLS CUI

C0040015;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [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)
- Abnormality of thrombocytes [HPO term]
- Qualitative platelet defects [ICD-10 Sub-category]
- Qualitative platelet defects [ICD-10 Sub-category (who)]
- THROMBOASTHENIA [WHO-ART Included Term]
- Thrombasthenia [PASCAL descriptor]
- haemophilia [Blood Transfusion thesaurus concept]
- qualitative platelet disorder, nos [SNOMED Notion]
Currated CISMeF NLP mapping
- Decreased platelet glycoprotein IIb-IIIa [HPO term]
- Glanzmann Thrombasthenia [NCIt concept]
- Glanzmann disease [Disease (Nov.)]
- Glanzmann thrombasthenia [PASCAL descriptor]
- Glanzmann thrombasthenia [ICD-11 More detail]
- Glanzmann thrombasthenia [ORDO Disease]
- Glanzmann thrombasthenia 1 [OMIM Phenotype]
- Glanzmann's disease [MedDRA Preferred Term]
- Glanzmann's disease [MedDRA LLT]
- Glanzmann's thrombasthenia [DO Concept]
- Glanzmann's thrombasthenia (disorder) [SNOMED CT concept]
- Hereditary thrombasthenia [MedDRA LLT]
- Thrombasthenia [HPO term]
- Thrombasthenia [MedDRA Preferred Term]
- hereditary thromboasthenia, nos [SNOMED Notion]
DO Cross reference
- Glanzmann's thrombasthenia [DO Concept]
HPO term
- Abnormality of thrombocytes [HPO term]
- Decreased platelet glycoprotein IIb-IIIa [HPO term]
Manual NTBT mappings (CISMeF)
- Fetal and neonatal alloimmune thrombocytopenia [ORDO Disease]
MeSH Descriptor(s) used for indexing
- platelet glycoprotein GPIIb-IIIa complex [MeSH Descriptor]
Record concept(s)
- thrombasthenia [MeSH concept]
Related MeSH Supplementary Concept(s)
- Thrombasthenia-Thrombocytopenia, hereditary [MeSH Supplementary Concept]
- glanzmann thrombasthenia, autosomal dominant [MeSH Supplementary Concept]
- schlegelberger grote syndrome [MeSH Supplementary Concept]
See also
- platelet glycoprotein GPIIb-IIIa complex [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Glanzmann Thrombasthenia [NCIt concept]
- Glanzmann disease [Disease (Nov.)]
- Glanzmann thrombasthenia [ORDO Disease]
- Glanzmann thrombasthenia 1 [OMIM Phenotype]
- Glanzmann's disease [MedDRA LLT]
- Glanzmann's disease [MedDRA Preferred Term]
- Glanzmann's thrombasthenia [DO Concept]
- Glanzmann's thrombasthenia (disorder) [SNOMED CT concept]
- Hereditary thrombasthenia [MedDRA LLT]
- THROMBOASTHENIA [WHO-ART Included Term]
- Thrombasthenia [HPO term]
- Thrombasthenia [MedDRA Preferred Term]
- Thromboasthenia [MedDRA LLT]
- hereditary thromboasthenia, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- Glanzmann thrombasthenia [OMIM phenotypic series]

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