Cystic Fibrosis [cystická fibróza]

topical
1 330
Terms

cystická fibróza pankreatu
cystická fibróza plic
fibrocystická nemoc slinivky břišní
mukoviscidóza

 

Cystic Fibrosis of Pancreas
Fibrocystic Disease of Pancreas
Mucoviscidosis
Pancreatic Cystic Fibrosis
Pulmonary Cystic Fibrosis

Persistent link   https://www.medvik.cz/link/D003550
Definition

An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.

Annotation
a specific disease entity: do not use for fibrocystic states of various organs
DUI
D003550 MeSH Browser
CUI
M0005551
History note
67; was PANCREATIC CYSTIC FIBROSIS 1963-66
Online note
use CYSTIC FIBROSIS to search PANCREATIC CYSTIC FIBROSIS 1966
Public note
67; was PANCREATIC CYSTIC FIBROSIS 1963-66

Allowable subheadings

BL
blood 30
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 4
CO
complications 250
DI
diagnosis 342
DG
diagnostic imaging 4
DH
diet therapy 19
DT
drug therapy 148
EC
economics 8
EM
embryology
EN
enzymology 6
EP
epidemiology 53
EH
ethnology 7
ET
etiology 60
GE
genetics 233
HI
history 12
IM
immunology 46
ME
metabolism 36
MI
microbiology 65
MO
mortality 19
NU
nursing 14
PS
parasitology
PA
pathology 67
PP
physiopathology 123
PC
prevention & control 43
PX
psychology 32
RT
radiotherapy
RH
rehabilitation 14
SU
surgery 18
TH
therapy 251
UR
urine 4
VE
veterinary
VI
virology

C Diseases
C06 Digestive System Diseases 674
C06.689 Pancreatic Diseases 620
C06.689.150 Congenital Hyperinsulinism 24
C06.689.202 Cystic Fibrosis 1 330
C06.689.276 Exocrine Pancreatic Insufficiency 65
C06.689.388 Pancreas Divisum
C06.689.500 Pancreatic Cyst 91
C06.689.583 Pancreatic Fistula 52
C06.689.667 Pancreatic Neoplasms 1 519
C06.689.750 Pancreatitis 1 351
C08 Respiratory Tract Diseases 2 223
C08.381 Lung Diseases 2 196
C08.381.074 Acute Chest Syndrome 2
C08.381.112 alpha 1-Antitrypsin Deficiency 86
C08.381.150 Cystic Adenomatoid Malformation of Lung, Congenital 9
C08.381.187 Cystic Fibrosis 1 330
C08.381.348 Hemoptysis 149
C08.381.367 Hemosiderosis, Pulmonary
C08.381.385 Hepatopulmonary Syndrome 8
C08.381.423 Hypertension, Pulmonary 1 370
C08.381.450 Lung Abscess 52
C08.381.472 Lung Diseases, Fungal 144
C08.381.483 Lung Diseases, Interstitial 424
C08.381.495 Lung Diseases, Obstructive 885
C08.381.517 Lung Diseases, Parasitic 24
C08.381.520 Lung Injury 136
C08.381.540 Lung Neoplasms 3 763
C08.381.570 Lung, Hyperlucent 2
C08.381.600 Plasma Cell Granuloma, Pulmonary 6
C08.381.677 Pneumonia 1 151
C08.381.719 Pulmonary Alveolar Proteinosis 28
C08.381.730 Pulmonary Atelectasis 78
C08.381.742 Pulmonary Edema 207
C08.381.746 Pulmonary Embolism 1 325
C08.381.750 Pulmonary Eosinophilia 40
C08.381.780 Pulmonary Veno-Occlusive Disease 10
C08.381.840 Respiratory Distress Syndrome 224
C08.381.844 Scimitar Syndrome 3
C08.381.884 Solitary Pulmonary Nodule 41
C08.381.922 Tuberculosis, Pulmonary 1 154
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
C16.320.080 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
C16.614 Infant, Newborn, Diseases 1 950
C16.614.042 Amniotic Band Syndrome 6
C16.614.053 Anemia, Neonatal 22
C16.614.092 Asphyxia Neonatorum 173
C16.614.131 Birth Injuries 158
C16.614.166 Colic 125
C16.614.183 Congenital Bone Marrow Failure Syndromes 2
C16.614.200 Congenital Hyperinsulinism 24
C16.614.213 Cystic Fibrosis 1 330
C16.614.258 Epilepsy, Benign Neonatal 13
C16.614.304 Erythroblastosis, Fetal 140
C16.614.378 Hernia, Umbilical 45
C16.614.438 Hydrophthalmos 9
C16.614.451 Hyperbilirubinemia, Neonatal 65
C16.614.465 Hyperostosis, Cortical, Congenital 14
C16.614.492 Ichthyosis 62
C16.614.521 Infant, Premature, Diseases 318
C16.614.580 Meconium Aspiration Syndrome 35
C16.614.595 Mobius Syndrome 10
C16.614.610 Neonatal Abstinence Syndrome 75
C16.614.627 Neonatal Sepsis 35
C16.614.643 Nystagmus, Congenital 8
C16.614.660 OEIS Complex
C16.614.677 Ophthalmia Neonatorum 12
C16.614.694 Persistent Fetal Circulation Syndrome 17
C16.614.760 Rothmund-Thomson Syndrome 8
C16.614.810 Sclerema Neonatorum 2
C16.614.815 Severe Combined Immunodeficiency 64
C16.614.868 Syphilis, Congenital 87
C16.614.890 Thanatophoric Dysplasia 7
C16.614.899 Thrombocytopenia, Neonatal Alloimmune 14
C16.614.909 Toxoplasmosis, Congenital 75
C16.614.940 Vitamin K Deficiency Bleeding 22
C16.614.947 Wolman Disease 15

Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Subnormal Mentality Disease MeSH Browser

Follicular hamartoma alopecia cystic fibrosis Disease MeSH Browser

Lubani Al Saleh Teebi syndrome Disease MeSH Browser

Add