alpha 1-Antitrypsin Deficiency [deficit alfa1-antitrypsinu]

topical
83
Terms

AATD
alfa-1-antitrypsin - nedostatečnost
deficit alfa-1 antitrypsinu
deficit alfa-1- antitrypsinu
deficit α1-antitrypsinu

Persistent link   https://www.medvik.cz/link/D019896
Definition

Deficiency of the protease inhibitor ALPHA 1-ANTITRYPSIN that manifests primarily as PULMONARY EMPHYSEMA and LIVER CIRRHOSIS.

Annotation
Pi or PiZZ goes here + PHENOTYPE
DUI
D019896 MeSH Browser
CUI
M0029552
Previous indexing
alpha 1-Antitrypsin (1974); alpha 1-Antitrypsin/deficiency (1975-1997)
History note
98
Public note
98

Allowable subheadings

BL
blood 4
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications 14
DI
diagnosis 37
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 30
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology 11
EH
ethnology
ET
etiology 3
GE
genetics 28
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality 1
NU
nursing
PS
parasitology
PA
pathology 8
PP
physiopathology 7
PC
prevention & control 1
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 15
UR
urine
VE
veterinary
VI
virology

C Diseases
C06 Digestive System Diseases 673
C06.552 Liver Diseases 3 016
C06.552.074 alpha 1-Antitrypsin Deficiency 83
C06.552.100 Chemical and Drug Induced Liver Injury 269
C06.552.150 Cholestasis, Intrahepatic 163
C06.552.241 Fatty Liver 368
C06.552.270 Focal Nodular Hyperplasia 18
C06.552.289 Hepatic Infarction
C06.552.308 Hepatic Insufficiency 39
C06.552.347 Budd-Chiari Syndrome 45
C06.552.360 Hepatic Veno-Occlusive Disease 23
C06.552.380 Hepatitis 734
C06.552.413 Hepatolenticular Degeneration 243
C06.552.416 Hepatomegaly 116
C06.552.455 Hepatopulmonary Syndrome 8
C06.552.465 Hepatorenal Syndrome 91
C06.552.494 Hypertension, Portal 647
C06.552.597 Liver Abscess 50
C06.552.630 Liver Cirrhosis 1 534
C06.552.645 Liver Diseases, Alcoholic 94
C06.552.664 Liver Diseases, Parasitic 56
C06.552.697 Liver Neoplasms 1 658
C06.552.802 Peliosis Hepatis
C06.552.830 Porphyrias, Hepatic 26
C06.552.933 Tuberculosis, Hepatic 9
C06.552.970 Zellweger Syndrome 10
C08 Respiratory Tract Diseases 2 218
C08.381 Lung Diseases 2 187
C08.381.074 Acute Chest Syndrome 2
C08.381.112 alpha 1-Antitrypsin Deficiency 83
C08.381.150 Cystic Adenomatoid Malformation of Lung, Congenital 9
C08.381.187 Cystic Fibrosis 1 328
C08.381.348 Hemoptysis 149
C08.381.367 Hemosiderosis, Pulmonary
C08.381.385 Hepatopulmonary Syndrome 8
C08.381.423 Hypertension, Pulmonary 1 365
C08.381.450 Lung Abscess 51
C08.381.472 Lung Diseases, Fungal 143
C08.381.483 Lung Diseases, Interstitial 421
C08.381.495 Lung Diseases, Obstructive 884
C08.381.517 Lung Diseases, Parasitic 24
C08.381.520 Lung Injury 136
C08.381.540 Lung Neoplasms 3 745
C08.381.570 Lung, Hyperlucent 2
C08.381.600 Plasma Cell Granuloma, Pulmonary 6
C08.381.677 Pneumonia 1 145
C08.381.719 Pulmonary Alveolar Proteinosis 26
C08.381.730 Pulmonary Atelectasis 78
C08.381.742 Pulmonary Edema 207
C08.381.746 Pulmonary Embolism 1 322
C08.381.750 Pulmonary Eosinophilia 40
C08.381.780 Pulmonary Veno-Occlusive Disease 10
C08.381.840 Respiratory Distress Syndrome 223
C08.381.844 Scimitar Syndrome 3
C08.381.884 Solitary Pulmonary Nodule 41
C08.381.922 Tuberculosis, Pulmonary 1 152
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
C16.320.077 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
C23 Pathological Conditions, Signs and Symptoms 451
C23.550 Pathologic Processes 195
C23.550.325 Emphysema 89
C23.550.325.500 Subcutaneous Emphysema 16
C23.550.325.500.500 alpha 1-Antitrypsin Deficiency 83

alpha-1-Antitrypsin Deficiency, Autosomal Recessive Disease MeSH Browser

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