loading...| Preferred Name |
obsolete_cystic fibrosis |
|
| Synonyms |
CF Cystic fibrosis (disorder) Cystic fibrosis without mention of meconium ileus Cystic fibrosis NOS cystic fibrosis with gastrointestinal manifestations Meconium obstruction of intestine in mucoviscidosis cystic fibrosis with pulmonary manifestations Fibrocystic disease cystic fibrosis with pulmonary manifestations (disorder) cystic fibrosis with other manifestations cystic fibrosis with meconium ileus (disorder) cystic fibrosis with other manifestations (disorder) CF - Cystic fibrosis mucoviscidosis Cystic fibrosis NOS (disorder) cystic fibrosis with combined manifestations CYSTIC FIBROS W/O ILEUS cystic fibrosis with meconium ileus Meconium ileus in cystic fibrosis (disorder) |
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| Definitions |
A congenital metabolic disorder affecting the exocrine glands, inherited as an autosomal trait. The secretions of exocrine glands are abnormal, resulting in excessively viscid mucus production which causes obstruction of passageways (including pancreatic and bile ducts, intestines, and bronchi). The sweat sodium and chloride content are increased. Symptoms usually appear in childhood and include meconium ileus, poor growth despite good appetite, malabsorption and foul bulky stools, chronic bronchitis with cough, recurrent pneumonia, bronchiectasis, emphysema, clubbing of the fingers, and salt depletion in hot weather. A congenital metabolic disorder affecting the exocrine glands, inherited as an autosomal trait. The secretions of exocrine glands are abnormal, resulting in excessively viscid mucus production which causes obstruction of passageways (including pancreatic and bile ducts, intestines, and bronchi). The sweat sodium and chloride content are increased. Symptoms usually appear in childhood and include meconium ileus, poor growth despite good appetite, malabsorption and foul bulky stools, chronic bronchitis with cough, recurrent pneumonia, bronchiectasis, emphysema, clubbing of the fingers, and salt depletion in hot weather. -- 2003 |
|
| ID |
http://www.ebi.ac.uk/efo/EFO_0000390 |
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| Obsolete |
true |
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| database_cross_reference |
OMIM:219700 SNOMEDCT:190911006 ICD9:277.00 SNOMEDCT:190905008 MeSH:D003550 DOID:1485 ICD9:277.0 NCIt:C2975 |
|
| definition |
A congenital metabolic disorder affecting the exocrine glands, inherited as an autosomal trait. The secretions of exocrine glands are abnormal, resulting in excessively viscid mucus production which causes obstruction of passageways (including pancreatic and bile ducts, intestines, and bronchi). The sweat sodium and chloride content are increased. Symptoms usually appear in childhood and include meconium ileus, poor growth despite good appetite, malabsorption and foul bulky stools, chronic bronchitis with cough, recurrent pneumonia, bronchiectasis, emphysema, clubbing of the fingers, and salt depletion in hot weather. A congenital metabolic disorder affecting the exocrine glands, inherited as an autosomal trait. The secretions of exocrine glands are abnormal, resulting in excessively viscid mucus production which causes obstruction of passageways (including pancreatic and bile ducts, intestines, and bronchi). The sweat sodium and chloride content are increased. Symptoms usually appear in childhood and include meconium ileus, poor growth despite good appetite, malabsorption and foul bulky stools, chronic bronchitis with cough, recurrent pneumonia, bronchiectasis, emphysema, clubbing of the fingers, and salt depletion in hot weather. -- 2003 |
|
| deprecated |
true |
|
| has_exact_synonym |
Meconium ileus in cystic fibrosis (disorder) cystic fibrosis with meconium ileus CYSTIC FIBROS W/O ILEUS cystic fibrosis with combined manifestations Cystic fibrosis NOS (disorder) mucoviscidosis CF - Cystic fibrosis cystic fibrosis with other manifestations (disorder) cystic fibrosis with meconium ileus (disorder) cystic fibrosis with other manifestations cystic fibrosis with pulmonary manifestations (disorder) Fibrocystic disease cystic fibrosis with pulmonary manifestations Meconium obstruction of intestine in mucoviscidosis cystic fibrosis with gastrointestinal manifestations Cystic fibrosis NOS Cystic fibrosis without mention of meconium ileus Cystic fibrosis (disorder) CF |
|
| label |
obsolete_cystic fibrosis |
|
| obsoleted_in_version |
2.32 |
|
| organizational_class |
true |
|
| prefixIRI |
efo1:EFO_0000390 |
|
| prefLabel |
obsolete_cystic fibrosis |
|
| reason_for_obsolescence |
use http://www.orpha.net/ORDO/Orphanet_586' instead. New Label : Cystic fibrosis |
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| term editor |
Tomasz Adamusiak James Malone |
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| term replaced by | ||
| subClassOf |