| CFS | cancer family syndrome; Chiari-Frommel syndrome; chronic fatigue syndrome; craniofacial stenosis; cr... |
|---|---|
| CFTR | cystic fibrosis transmembrane conductance regulator |
| CH | case history; Chediak-Higashi [syndrome]; chiasma; Chinese hamster; chloral hydrate; cholesterol; Ch... |
| CMN | caudal mediastinal node; cystic medial necrosis |
| CMN-AA | cystic medial necrosis of ascending aorta |
| CAM | cystic adenomatoid malformation |
|---|---|
| CFTR | cystic fibrosis transmembrane conductance regulator protein |
| cysticolithotripsy |
(cys
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
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|---|---|
| cysticorrhaphy |
(cys
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
|
| cystic fibrosis |
a disease in which the body produces thick, sticky mucus that affects the lungs and pancreas. This leads to breathing problems, frequent lung infections, poor weight gain and other problems. The average life expectancy of someone with cystic fibrosis is age 30.
Ãâó: https://www.healthforums.com/library/1,1277,articl...
|
| cystic fibrosis |
A potentially lethal human disease of secretory cells, showing excess lung mucus secretion, and inherited as an autosomal recessive on chromosome 7. CF is caused by mutations in a gene encoding the cystic fibrosis membrane conductance regulator, a transmembrane protein involved in ion transport.
Ãâó: helios.bto.ed.ac.uk/bto/glossary/c2.htm
|
| cystic fibrosis |
Hereditary disease whose symptoms usually appear shortly after birth. They include faulty digestion, breathing difficulties and respiratory infections due to mucus accumulation, and excessive loss of salt in sweat. In the past, cystic fibrosis was almost always fatal in childhood, but treatment is now so improved that patients commonly live to their 20s and beyond.
Ãâó: science.education.nih.gov/supplements/nih1/genetic...
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