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Hemoglobinopathies [hemoglobinopatie]

topical

68

Persistent link https://www.medvik.cz/link/D006453

Definition

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

DUI: D006453 MeSH Browser
CUI: M0010129
History note: 68
Public note: 68

Allowable subheadings

... Occurrences in Medvik records

C Diseases

C15 Hemic and Lymphatic Diseases 91

C15.378 Hematologic Diseases 975

C15.378.050 Anemia 1 249

C15.378.100 Blood Coagulation Disorders 600

C15.378.140 Blood Platelet Disorders 123

C15.378.147 Blood Protein Disorders 126

C15.378.190 Bone Marrow Diseases 187

C15.378.243 Cytopenia 3

C15.378.295 Erythroblastosis, Fetal 140

C15.378.400 Hematologic Neoplasms 869

C15.378.420 Hemoglobinopathies 68

C15.378.420.155 Anemia, Sickle Cell 45

C15.378.420.463 Hemoglobin C Disease 1

C15.378.420.826 Thalassemia 85

C15.378.463 Hemorrhagic Disorders 95

C15.378.508 Leukemia 1 359

C15.378.553 Leukocyte Disorders 18

C15.378.619 Methemoglobinemia 79

C15.378.738 Polycythemia 109

C15.378.785 Pregnancy Complications, Hematologic 251

C15.378.800 Preleukemia 13

C15.378.896 Sulfhemoglobinemia 2

C15.378.925 Thrombophilia 425

C15.378.962 Transfusion Reaction 235

C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439

C16.320 Genetic Diseases, Inborn 1 214

C16.320.033 Adrenal Hyperplasia, Congenital 226

C16.320.051 Alagille Syndrome 19

C16.320.060 alpha 1-Antitrypsin Deficiency 86

C16.320.070 Anemia, Hemolytic, Congenital 48

C16.320.077 Anemia, Hypoplastic, Congenital 3

C16.320.080 Ataxia Telangiectasia 47

C16.320.089 Autoimmune Lymphoproliferative Syndrome 2

C16.320.099 Blood Coagulation Disorders, Inherited 64

C16.320.100 Brugada Syndrome 40

C16.320.129 CADASIL 8

C16.320.144 Camurati-Engelmann Syndrome 6

C16.320.160 Cardiomyopathy, Hypertrophic, Familial 33

C16.320.165 CHARGE Syndrome 1

C16.320.170 Cherubism 1

C16.320.180 Chromosome Disorders 259

C16.320.184 Ciliopathies 9

C16.320.188 Costello Syndrome 3

C16.320.190 Cystic Fibrosis 1 330

C16.320.215 Donohue Syndrome 1

C16.320.240 Dwarfism 99

C16.320.290 Eye Diseases, Hereditary 57

C16.320.298 Familial Multiple Lipomatosis

C16.320.306 Frasier Syndrome

C16.320.314 GATA2 Deficiency 2

C16.320.322 Genetic Diseases, X-Linked 60

C16.320.338 Genetic Diseases, Y-Linked 1

C16.320.355 Hajdu-Cheney Syndrome 6

C16.320.365 Hemoglobinopathies 68

C16.320.365.155 Anemia, Sickle Cell 45

C16.320.365.463 Hemoglobin C Disease 1

C16.320.365.826 Thalassemia 85

C16.320.382 Hereditary Autoinflammatory Diseases 46

C16.320.400 Heredodegenerative Disorders, Nervous System 45

C16.320.413 Hyper-IgM Immunodeficiency Syndrome 4

C16.320.427 Hyperthyroxinemia, Familial Dysalbuminemic 2

C16.320.447 Imprinting Disorders

C16.320.467 Kallmann Syndrome 10

C16.320.480 Kartagener Syndrome 46

C16.320.488 Laminopathies 2

C16.320.495 Lennox Gastaut Syndrome 5

C16.320.510 Loeys-Dietz Syndrome 7

C16.320.540 Marfan Syndrome 105

C16.320.565 Metabolism, Inborn Errors 711

C16.320.577 Muscular Dystrophies 140

C16.320.590 Myasthenic Syndromes, Congenital 20

C16.320.600 Nail-Patella Syndrome 8

C16.320.700 Neoplastic Syndromes, Hereditary 144

C16.320.709 Oculocerebrorenal Syndrome 9

C16.320.714 Orofaciodigital Syndromes 7

C16.320.718 Osteoarthropathy, Primary Hypertrophic 127

C16.320.728 Osteochondrodysplasias 125

C16.320.737 Osteogenesis Imperfecta 106

C16.320.775 Pain Insensitivity, Congenital 10

C16.320.784 Pelger-Huet Anomaly 7

C16.320.798 Primary Immunodeficiency Diseases 48

C16.320.812 Pycnodysostosis 2

C16.320.831 Renal Tubular Transport, Inborn Errors 36

C16.320.850 Skin Diseases, Genetic 89

C16.320.925 Werner Syndrome 14

C16.320.962 Yellow Nail Syndrome

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