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Hemoglobinopathies
MeSH Descriptor Data 2025
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Hemoglobinopathies
Tree Number(s)
C15.378.420
C16.320.365
Unique ID
D006453
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D006453
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
Scope Note
A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.
NLM Classification #
WH 190
See Also
Hemoglobins, Abnormal
Public MeSH Note
68
History Note
68
Date Established
1968/01/01
Date of Entry
1999/01/01
Revision Date
2001/07/25
Allowable Qualifiers
blood (BL)
cerebrospinal fluid (CF)
chemically induced (CI)
classification (CL)
complications (CO)
diagnosis (DI)
diagnostic imaging (DG)
diet therapy (DH)
drug therapy (DT)
economics (EC)
embryology (EM)
enzymology (EN)
epidemiology (EP)
ethnology (EH)
etiology (ET)
genetics (GE)
history (HI)
immunology (IM)
metabolism (ME)
microbiology (MI)
mortality (MO)
nursing (NU)
parasitology (PS)
pathology (PA)
physiopathology (PP)
prevention & control (PC)
psychology (PX)
radiotherapy (RT)
rehabilitation (RH)
surgery (SU)
therapy (TH)
urine (UR)
veterinary (VE)
virology (VI)
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Anemia [C15.378.050]
Blood Coagulation Disorders [C15.378.100]
Blood Platelet Disorders [C15.378.140]
Blood Protein Disorders [C15.378.147]
Bone Marrow Diseases [C15.378.190]
Cytopenia [C15.378.243]
Erythroblastosis, Fetal [C15.378.295]
Hematologic Neoplasms [C15.378.400]
Hemoglobinopathies [C15.378.420]
Anemia, Sickle Cell [C15.378.420.155]
Hemoglobin C Disease [C15.378.420.463]
Thalassemia [C15.378.420.826]
Hemorrhagic Disorders [C15.378.463]
Leukemia [C15.378.508]
Leukocyte Disorders [C15.378.553]
Methemoglobinemia [C15.378.619]
Polycythemia [C15.378.738]
Pregnancy Complications, Hematologic [C15.378.785]
Preleukemia [C15.378.800]
Sulfhemoglobinemia [C15.378.896]
Thrombophilia [C15.378.925]
Transfusion Reaction [C15.378.962]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Adrenal Hyperplasia, Congenital [C16.320.033]
Alagille Syndrome [C16.320.051]
alpha 1-Antitrypsin Deficiency [C16.320.060]
Anemia, Hemolytic, Congenital [C16.320.070]
Anemia, Hypoplastic, Congenital [C16.320.077]
Ataxia Telangiectasia [C16.320.080]
Autoimmune Lymphoproliferative Syndrome [C16.320.089]
Blood Coagulation Disorders, Inherited [C16.320.099]
Brugada Syndrome [C16.320.100]
CADASIL [C16.320.129]
Camurati-Engelmann Syndrome [C16.320.144]
Cardiomyopathy, Hypertrophic, Familial [C16.320.160]
CHARGE Syndrome [C16.320.165]
Cherubism [C16.320.170]
Chromosome Disorders [C16.320.180]
Ciliopathies [C16.320.184]
Costello Syndrome [C16.320.188]
Cystic Fibrosis [C16.320.190]
Donohue Syndrome [C16.320.215]
Dwarfism [C16.320.240]
Eye Diseases, Hereditary [C16.320.290]
Familial Multiple Lipomatosis [C16.320.298]
Frasier Syndrome [C16.320.306]
GATA2 Deficiency [C16.320.314]
Genetic Diseases, X-Linked [C16.320.322]
Genetic Diseases, Y-Linked [C16.320.338]
Hajdu-Cheney Syndrome [C16.320.355]
Hemoglobinopathies [C16.320.365]
Anemia, Sickle Cell [C16.320.365.155]
Hemoglobin C Disease [C16.320.365.463]
Thalassemia [C16.320.365.826]
Hereditary Autoinflammatory Diseases [C16.320.382]
Heredodegenerative Disorders, Nervous System [C16.320.400]
Hyper-IgM Immunodeficiency Syndrome [C16.320.413]
Hyperthyroxinemia, Familial Dysalbuminemic [C16.320.427]
Imprinting Disorders [C16.320.447]
Kallmann Syndrome [C16.320.467]
Kartagener Syndrome [C16.320.480]
Laminopathies [C16.320.488]
Lennox Gastaut Syndrome [C16.320.495]
Loeys-Dietz Syndrome [C16.320.510]
Marfan Syndrome [C16.320.540]
Metabolism, Inborn Errors [C16.320.565]
Muscular Dystrophies [C16.320.577]
Myasthenic Syndromes, Congenital [C16.320.590]
Nail-Patella Syndrome [C16.320.600]
Neoplastic Syndromes, Hereditary [C16.320.700]
Oculocerebrorenal Syndrome [C16.320.709]
Orofaciodigital Syndromes [C16.320.714]
Osteoarthropathy, Primary Hypertrophic [C16.320.718]
Osteochondrodysplasias [C16.320.728]
Osteogenesis Imperfecta [C16.320.737]
Pain Insensitivity, Congenital [C16.320.775]
Pelger-Huet Anomaly [C16.320.784]
Primary Immunodeficiency Diseases [C16.320.798]
Pycnodysostosis [C16.320.812]
Renal Tubular Transport, Inborn Errors [C16.320.831]
Skin Diseases, Genetic [C16.320.850]
Werner Syndrome [C16.320.925]
Yellow Nail Syndrome [C16.320.962]
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Hemoglobinopathies
Preferred
Concept UI
M0010129
Scope Note
A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.
Terms
Hemoglobinopathies
Preferred Term
Term UI
T019485
Date
01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1968)
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