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Anemia, Hypoplastic, Congenital [hypoplastická kongenitální anemie]

topical

3

Terms: anemie hypoplastická kongenitální
anémie hypoplastická kongenitální
chronická kongenitální erythrogenesis imperfecta
Diamondova-Blackfanova anémie

: Congenital Hypoplastic Anemia
Hypoplastic Anemia, Congenital

Persistent link https://www.medvik.cz/link/D029502

Definition

An inborn condition characterized by deficiencies of red cell precursors that sometimes also includes LEUKOPENIA and THROMBOCYTOPENIA.

DUI: D029502 MeSH Browser
CUI: M0384816
Previous indexing: Fanconi Anemia (1992-2001); Anemia, Aplastic (1970-1991)
History note: 2002; use FANCONI ANEMIA 1992-2001
Public note: 2002;see FANCONI ANEMIA 1992-2001

Allowable subheadings

... Occurrences in Medvik records

C Diseases

C15 Hemic and Lymphatic Diseases 91

C15.378 Hematologic Diseases 976

C15.378.050 Anemia 1 249

C15.378.050.085 Anemia, Aplastic 207

C15.378.050.085.080 Anemia, Hypoplastic, Congenital 3

C15.378.050.085.080.090 Anemia, Diamond-Blackfan 42

C15.378.050.085.080.280 Fanconi Anemia 46

C15.378.190 Bone Marrow Diseases 187

C15.378.190.223 Bone Marrow Failure Disorders 6

C15.378.190.223.500 Congenital Bone Marrow Failure Syndromes 2

C15.378.190.223.500.500 Anemia, Hypoplastic, Congenital 3

C15.378.190.223.500.500.090 Anemia, Diamond-Blackfan 42

C15.378.190.223.500.500.280 Fanconi Anemia 46

C15.378.190.223.500.750 Dyskeratosis Congenita 9

C15.378.190.223.500.875 Shwachman-Diamond Syndrome 2

C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439

C16.320 Genetic Diseases, Inborn 1 215

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

C16.320.077.090 Anemia, Diamond-Blackfan 42

C16.320.077.280 Fanconi Anemia 46

C16.320.080 Ataxia Telangiectasia 48

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 260

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 58

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

C16.320.382 Hereditary Autoinflammatory Diseases 47

C16.320.400 Heredodegenerative Disorders, Nervous System 46

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 6

C16.320.510 Loeys-Dietz Syndrome 7

C16.320.540 Marfan Syndrome 105

C16.320.565 Metabolism, Inborn Errors 714

C16.320.577 Muscular Dystrophies 141

C16.320.590 Myasthenic Syndromes, Congenital 21

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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