Cystic fibrosis, other manifestations/unspecified

Description

obsolete_cystic fibrosis: ['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', '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.']

Data source
FinnGen phenocode E4_CYSTFIBRO_NAS
Hospital Discharge registry ICD-10: E849/E848, ICD-8: 2730
Cause of Death registry ICD-10: E848/E849, ICD-8: 2730
Level in the ICD-hierarchy 4
First defined in version DF2
Ontology
DOID 1485
GWAS catalog 0000390

Key figures

Sex All Female Male
Number of individuals 10 7 N/A
Unadjusted prevalence (%) 0.01 0.01 N/A
Mean age at first event (years) 37.04 40.79 N/A
Median number of events / individual 1 2 N/A

Clinical metrics

Sex All Female Male
Recurrence within 6 months (%) 50.0 57.14 N/A
Case fatality at 5-years (%) 0.0 0.0 N/A

Associations