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Descriptor English: Hemoglobinopathies
Descriptor Spanish: Hemoglobinopatías
Descriptor hemoglobinopatías
Scope note: Grupo de trastornos hereditarios que se caracterizan por alteraciones estructurales en la molécula de hemoglobina.
Descriptor Portuguese: Hemoglobinopatias
Descriptor French: Hémoglobinopathies
Entry term(s): Maladies de l'hémoglobine
Tree number(s): C15.378.420
C16.320.365
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D006453
Scope note: A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.
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
Allowable Qualifiers: BL sang
CF liquide cérébrospinal
CI induit chimiquement
CL classification
CO complications
DG imagerie diagnostique
DH diétothérapie
DI diagnostic
DT traitement médicamenteux
EC économie
EH ethnologie
EM embryologie
EN enzymologie
EP épidémiologie
ET étiologie
GE génétique
HI histoire
IM immunologie
ME métabolisme
MI microbiologie
MO mortalité
NU soins infirmiers
PA anatomopathologie
PC prévention et contrôle
PP physiopathologie
PS parasitologie
PX psychologie
RH rééducation et réadaptation
RT radiothérapie
SU chirurgie
TH thérapie
UR urine
VE médecine vétérinaire
VI virologie
Related: Hémoglobines anormales MeSH
DeCS ID: 6603
Unique ID: D006453
NLM Classification: WH 190
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1968/01/01
Date of Entry: 1999/01/01
Revision Date: 2001/07/25
Hémoglobinopathies - Preferred
Concept UI M0010129
Preferred term Hémoglobinopathies
Entry term(s) Maladies de l'hémoglobine



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