hemoglobinopathies

Preferred Label : hemoglobinopathies;

MeSH definition : A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.;

MeSH synonym : hemoglobinopathy;

MeSH annotation : do not confuse with HEMOGLOBINS, ABNORMAL (D12): use term in the text; coord IM with specific abnormal hemoglobin (IM) but HEMOGLOBIN C DISEASE; THALASSEMIA (hemoglobin H disease) & ANEMIA, SICKLE CELL (hemoglobin S disease) are available;

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

Details

Origin ID

D006453;

UMLS CUI

C0019045;

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)
- Other haemoglobinopathies [ICD-10 Sub-category (who)]
- Other haemoglobinopathies [MedDRA LLT]
- Other hemoglobinopathies [LOINC component]
Currated CISMeF NLP mapping
- Haemoglobinopathies [MedDRA High Level Group Term]
- Haemoglobinopathy [MedDRA Preferred Term]
- Haemoglobinopathy NOS [MedDRA LLT]
- Hemoglobin disorders [LOINC component]
- Hemoglobinopathy [PASCAL descriptor]
- Hemoglobinopathy [TUV Concept]
- Hemoglobinopathy [TUV Term]
- Hemoglobinopathy [NCIt concept]
- Hemoglobinopathy [ORDO Disease]
- Hemoglobinopathy [MedDRA LLT]
- Hemoglobinopathy (disorder) [SNOMED CT concept]
- hemoglobinopathy [DO Concept]
- hemoglobinopathy [Disease (Nov.)]
- hemoglobinopathy [Blood Transfusion thesaurus concept]
- hemoglobinopathy, nos [SNOMED Notion]
DO Cross reference
- hemoglobinopathy [DO Concept]
Manual BTNT mappings - CISMeF
- Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Rare anemia [ORDO Disease]
- Rare constitutional anemia [ORDO Disease]
ORDO relation(s)
- Hemoglobinopathy [ORDO Disease]
Record concept(s)
- hemoglobinopathies [MeSH concept]
See also
- hemoglobins, abnormal [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Haemoglobinopathies [MedDRA High Level Group Term]
- Haemoglobinopathies congenital [MedDRA High Level Term]
- Haemoglobinopathy [MedDRA Preferred Term]
- Haemoglobinopathy NOS [MedDRA LLT]
- Hemoglobin disorders [LOINC component]
- Hemoglobinopathy [MedDRA LLT]
- Hemoglobinopathy [ORDO Disease]
- Hemoglobinopathy [TUV Concept]
- Hemoglobinopathy [TUV Term]
- Hemoglobinopathy [PASCAL descriptor]
- Hemoglobinopathy [NCIt concept]
- Hemoglobinopathy (disorder) [SNOMED CT concept]
- hemoglobinopathy [DO Concept]
- hemoglobinopathy [Disease (Nov.)]
- hemoglobinopathy, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients