Anemia, Hemolytic, Congenital [kongenitální hemolytická anemie]

topical
48
Terms

anemie hemolytická kongenitální
anémie hemolytická kongenitální
dědičná hemolytická anemie
hemolytická anemie kongenitální

 

Anemia, Hemolytic, Hereditary
Congenital Hemolytic Anemia
Hemolytic Anemia, Congenital
Hemolytic Anemia, Hereditary
Hereditary Hemolytic Anemia

Persistent link   https://www.medvik.cz/link/D000745
Definition

Hemolytic anemia due to various intrinsic defects of the erythrocyte.

DUI
D000745 MeSH Browser
CUI
M0001129
History note
68; was ANEMIA, CONGENITAL HEMOLYTIC 1965-67, was ANEMIA, CONGENITAL HEMOLYTIC see SPHEROCYTOSIS, HEREDITARY 1963-64
Online note
use ANEMIA, HEMOLYTIC, CONGENITAL to search ANEMIA, CONGENITAL HEMOLYTIC 1966-67
Public note
68; was ANEMIA, CONGENITAL HEMOLYTIC 1965-67, was ANEMIA, CONGENITAL HEMOLYTIC see SPHEROCYTOSIS, HEREDITARY 1963-64; ANEMIA, HEMOLYTIC, CONGENITAL NONSPHEROCYTIC was heading 1968-81, was ANEMIA, CONGENITAL NON-SPHEROCYTIC HEMOLYTIC 1965-67

Allowable subheadings

BL
blood 2
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 2
CO
complications 1
DI
diagnosis 9
DG
diagnostic imaging
DH
diet therapy 1
DT
drug therapy 3
EC
economics
EM
embryology
EN
enzymology 1
EP
epidemiology 2
EH
ethnology
ET
etiology 4
GE
genetics 7
HI
history
IM
immunology 1
ME
metabolism 1
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 2
PP
physiopathology 1
PC
prevention & control 8
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery 1
TH
therapy 9
UR
urine
VE
veterinary
VI
virology

C Diseases
C15 Hemic and Lymphatic Diseases 91
C15.378 Hematologic Diseases 975
C15.378.050 Anemia 1 245
C15.378.050.141 Anemia, Hemolytic 257
C15.378.050.141.125 Anemia, Hemolytic, Autoimmune 89
C15.378.050.141.150 Anemia, Hemolytic, Congenital 48
C15.378.050.141.150.095 Anemia, Dyserythropoietic, Congenital 16
C15.378.050.141.150.100 Anemia, Hemolytic, Congenital Nonspherocytic 13
C15.378.050.141.150.150 Anemia, Sickle Cell 45
C15.378.050.141.150.365 Elliptocytosis, Hereditary 6
C15.378.050.141.150.480 Glucosephosphate Dehydrogenase Deficiency 15
C15.378.050.141.150.490 Hemoglobin C Disease 1
C15.378.050.141.150.785 Spherocytosis, Hereditary 43
C15.378.050.141.150.875 Thalassemia 85
C15.378.050.141.370 Favism 6
C15.378.050.141.560 Hemoglobinuria, Paroxysmal 82
C15.378.050.141.610 Hemolytic-Uremic Syndrome 180
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.033 Adrenal Hyperplasia, Congenital 225
C16.320.051 Alagille Syndrome 19
C16.320.060 alpha 1-Antitrypsin Deficiency 83
C16.320.070 Anemia, Hemolytic, Congenital 48
C16.320.070.095 Anemia, Dyserythropoietic, Congenital 16
C16.320.070.100 Anemia, Hemolytic, Congenital Nonspherocytic 13
C16.320.070.150 Anemia, Sickle Cell 45
C16.320.070.365 Elliptocytosis, Hereditary 6
C16.320.070.480 Glucosephosphate Dehydrogenase Deficiency 15
C16.320.070.490 Hemoglobin C Disease 1
C16.320.070.785 Spherocytosis, Hereditary 43
C16.320.070.875 Thalassemia 85
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 61
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
C16.320.144 Camurati-Engelmann Syndrome 6
C16.320.160 Cardiomyopathy, Hypertrophic, Familial 32
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 1 328
C16.320.215 Donohue Syndrome 1
C16.320.240 Dwarfism 97
C16.320.290 Eye Diseases, Hereditary 57
C16.320.298 Familial Multiple Lipomatosis
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 1
C16.320.322 Genetic Diseases, X-Linked 59
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 46
C16.320.400 Heredodegenerative Disorders, Nervous System 45
C16.320.413 Hyper-IgM Immunodeficiency Syndrome 4
C16.320.427 Hyperthyroxinemia, Familial Dysalbuminemic 1
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 143
C16.320.709 Oculocerebrorenal Syndrome 9
C16.320.714 Orofaciodigital Syndromes 7
C16.320.718 Osteoarthropathy, Primary Hypertrophic 127
C16.320.728 Osteochondrodysplasias 123
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 46
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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