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

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

http://www.ebi.ac.uk/efo/EFO_0000390

true

OMIM:219700

SNOMEDCT:190911006

ICD9:277.00

SNOMEDCT:190905008

MeSH:D003550

DOID:1485

ICD9:277.0

NCIt:C2975

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

true

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

obsolete_cystic fibrosis

2.32

true

obsolete_cystic fibrosis

efo:EFO_0000390

obsolete_cystic fibrosis

use http://www.orpha.net/ORDO/Orphanet_586' instead. New Label : Cystic fibrosis

Tomasz Adamusiak

James Malone

http://www.orpha.net/ORDO/Orphanet_586

http://www.w3.org/2002/07/owl#Thing