thalassemia - CISMeF

Preferred Label : thalassemia;

MeSH definition : A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.;

MeSH synonym : thalassemias;

MeSH annotation : a congen hemolytic anemia; GEN or unspecified: prefer specifics; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; general or unspecified; prefer specifics;

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

Details

Origin ID

D013789;

UMLS CUI

C0039730;

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)
- Thalassaemia, unspecified [ICD-10 Sub-category (who)]
- hereditary haemolytic anaemia [ICPC-2 Rubric]
- α δ-Thalassemia [PASCAL descriptor]
- α-Thalassemia [PASCAL descriptor]
- β δ-Thalassemia [PASCAL descriptor]
- β-Thalassemia [PASCAL descriptor]
Currated CISMeF NLP mapping
- Imbalanced hemoglobin synthesis [HPO term]
- Thalassaemia [ICD-10 category (who)]
- Thalassaemia [MedDRA Preferred Term]
- Thalassaemia NOS [MedDRA LLT]
- Thalassaemias [ICD-11 Category]
- Thalassemia [ICD-10 category]
- Thalassemia [PASCAL descriptor]
- Thalassemia [NCIt concept]
- Thalassemia [MedDRA LLT]
- Thalassemia (disorder) [SNOMED CT concept]
- Thalassemias [ICD-9 code]
- thalassemia [Disease (Nov.)]
- thalassemia [DO Concept]
- thalassemia [MedlinePlus Topic]
- thalassemia [Blood Transfusion thesaurus concept]
- thalassemia [medical devices type]
- thalassemia [Radlex concept]
- thalassemia, nos [SNOMED Notion]
DO Cross reference
- thalassemia [DO Concept]
False automatic mappings
- Other thalassaemias [ICD-10 Sub-category (who)]
Indexing information
- hemoglobin medicine lake [MeSH Supplementary Concept]
MedlinePlus topic(s)
- thalassemia [MedlinePlus Topic]
Record concept(s)
- thalassemia [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Thalassaemia [ICD-10 category (who)]
- Thalassaemia [MedDRA Preferred Term]
- Thalassaemia NOS [MedDRA LLT]
- Thalassaemic disorders [MedDRA High Level Term]
- Thalassemia [MedDRA LLT]
- Thalassemia [ICD-10 category]
- Thalassemia [NCIt concept]
- Thalassemia (disorder) [SNOMED CT concept]
- Thalassemia syndrome (disorder) [SNOMED CT concept]
- Thalassemia, unspecified [ICD-9 code]
- Thalassemia, unspecified [ICD-10 Sub-category]
- Thalassemias [ICD-9 code]
- thalassemia [DO Concept]
- thalassemia [Disease (Nov.)]
- thalassemia [MedlinePlus Topic]
- thalassemia syndrome, nos [SNOMED Notion]
- thalassemia, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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