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Regulation of Gene Expression Ontolology
Last uploaded:
December 16, 2015
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| Id | http://identifiers.org/omim/219700
http://identifiers.org/omim/219700
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|---|---|
| Preferred Name | Cystic fibrosis |
| Definitions |
(CF) - A common generalized disorder of the exocrine glands which impairs clearance of secretions in a variety of organs. It is characterized by the triad of chronic bronchopulmonary disease (with recurrent respiratory infections), pancreatic insufficiency (which leads to malabsorption and growth retardation) and elevated sweat electrolytes. It is the most common genetic disease in Caucasians, with a prevalence of about 1 in 2'000 live births. Inheritance is autosomal recessive.
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| Synonyms |
CF
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | (CF) - A common generalized disorder of the exocrine glands which impairs clearance of secretions in a variety of organs. It is characterized by the triad of chronic bronchopulmonary disease (with recurrent respiratory infections), pancreatic insufficiency (which leads to malabsorption and growth retardation) and elevated sweat electrolytes. It is the most common genetic disease in Caucasians, with a prevalence of about 1 in 2'000 live births. Inheritance is autosomal recessive. |
|---|---|
| altLabel |
CF
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| prefLabel |
Cystic fibrosis
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| notation |
OMIM:219700
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| id |
OMIM:219700
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| subClassOf | |
| type |
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