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alpha 1-Antitrypsin Deficiency
MeSH Descriptor Data 2024
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
alpha 1-Antitrypsin Deficiency
Tree Number(s)
C06.552.074
C08.381.112
C16.320.060
C23.550.325.500.500
Unique ID
D019896
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D019896
Annotation
Pi or PiZZ goes here +
PHENOTYPE
Scope Note
Deficiency of the protease inhibitor
ALPHA 1-ANTITRYPSIN
that manifests primarily as
PULMONARY EMPHYSEMA
and
LIVER CIRRHOSIS
.
Entry Version
ALPHA 1 ANTITRYPSIN DEFIC
Previous Indexing
alpha 1-Antitrypsin (1974)
alpha 1-Antitrypsin/deficiency (1975-1997)
Public MeSH Note
98
History Note
98
Date Established
1998/01/01
Date of Entry
1997/06/20
Revision Date
2013/07/08
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)
Digestive System Diseases [C06]
Liver Diseases [C06.552]
alpha 1-Antitrypsin Deficiency [C06.552.074]
Chemical and Drug Induced Liver Injury [C06.552.100]
Cholestasis, Intrahepatic [C06.552.150]
Fatty Liver [C06.552.241]
Focal Nodular Hyperplasia [C06.552.270]
Hepatic Infarction [C06.552.289]
Hepatic Insufficiency [C06.552.308]
Budd-Chiari Syndrome [C06.552.347]
Hepatic Veno-Occlusive Disease [C06.552.360]
Hepatitis [C06.552.380]
Hepatolenticular Degeneration [C06.552.413]
Hepatomegaly [C06.552.416]
Hepatopulmonary Syndrome [C06.552.455]
Hepatorenal Syndrome [C06.552.465]
Hypertension, Portal [C06.552.494]
Liver Abscess [C06.552.597]
Liver Cirrhosis [C06.552.630]
Liver Diseases, Alcoholic [C06.552.645]
Liver Diseases, Parasitic [C06.552.664]
Liver Neoplasms [C06.552.697]
Peliosis Hepatis [C06.552.802]
Porphyrias, Hepatic [C06.552.830]
Tuberculosis, Hepatic [C06.552.933]
Zellweger Syndrome [C06.552.970]
Respiratory Tract Diseases [C08]
Lung Diseases [C08.381]
Acute Chest Syndrome [C08.381.074]
alpha 1-Antitrypsin Deficiency [C08.381.112]
Cystic Adenomatoid Malformation of Lung, Congenital [C08.381.150]
Cystic Fibrosis [C08.381.187]
Hemoptysis [C08.381.348]
Hemosiderosis, Pulmonary [C08.381.367]
Hepatopulmonary Syndrome [C08.381.385]
Hypertension, Pulmonary [C08.381.423]
Lung Abscess [C08.381.450]
Lung Diseases, Fungal [C08.381.472]
Lung Diseases, Interstitial [C08.381.483]
Lung Diseases, Obstructive [C08.381.495]
Lung Diseases, Parasitic [C08.381.517]
Lung Injury [C08.381.520]
Lung Neoplasms [C08.381.540]
Lung, Hyperlucent [C08.381.570]
Plasma Cell Granuloma, Pulmonary [C08.381.600]
Pneumonia [C08.381.677]
Pulmonary Alveolar Proteinosis [C08.381.719]
Pulmonary Atelectasis [C08.381.730]
Pulmonary Edema [C08.381.742]
Pulmonary Embolism [C08.381.746]
Pulmonary Eosinophilia [C08.381.750]
Pulmonary Veno-Occlusive Disease [C08.381.780]
Respiratory Distress Syndrome [C08.381.840]
Scimitar Syndrome [C08.381.844]
Solitary Pulmonary Nodule [C08.381.884]
Tuberculosis, Pulmonary [C08.381.922]
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]
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]
Pathological Conditions, Signs and Symptoms [C23]
Pathologic Processes [C23.550]
Emphysema [C23.550.325]
Subcutaneous Emphysema [C23.550.325.500]
alpha 1-Antitrypsin Deficiency [C23.550.325.500.500]
Expand All
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alpha 1-Antitrypsin Deficiency
Preferred
Concept UI
M0029552
Scope Note
Deficiency of the protease inhibitor
ALPHA 1-ANTITRYPSIN
that manifests primarily as
PULMONARY EMPHYSEMA
and
LIVER CIRRHOSIS
.
Terms
alpha 1-Antitrypsin Deficiency
Preferred Term
Term UI
T059262
Date
01/01/1999
LexicalTag
NON
ThesaurusID
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