cystic fibrosis
ICD-10: E84MeSH: D003550ORPHA: 586
Overview
autosomal recessive disease characterized by the buildup of mucus
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with cystic fibrosis, sourced from HPO and Orphanet clinical annotations.
DepressionAnxietyOsteopeniaAbnormality of the liverGastroesophageal refluxRectal prolapseAsthmaSteatorrheaRecurrent Aspergillus infectionsRecurrent Staphylococcus aureus infectionsRecurrent lower respiratory tract infectionsElevated circulating hepatic transaminase concentrationMeconium ileusRecurrent Haemophilus influenzae infectionsReduced forced expiratory volume in one secondDecreased body mass indexHearing impairmentNephrolithiasisOsteoporosisCirrhosisHemoptysisPneumothoraxRecurrent Burkholderia cepacia infectionsNontuberculous mycobacterial pulmonary infectionNasal polyposisExocrine pancreatic insufficiencyMalabsorptionBronchiectasisRecurrent respiratory infectionsAirway obstructionElevated sweat chlorideAbsent vas deferensFailure to thriveMale infertilitySinusitisPneumoniaPulmonary fibrosisHepatitisLiver cirrhosisPeptic ulcer diseaseHeart failureBronchitisDyspneaCyanosisMuscle weaknessGallstoneAtelectasisCholestasisBowel obstruction
Classification & Codes
ICD-10 Code
E84MeSH Code
D003550Orphanet Code
ORPHA:586cystic fibrosis
| ICD-10 | E84 |
| MeSH | D003550 |
| Orphanet | ORPHA:586 |
| Treatments | 0 drug(s) |
| Symptoms on record | 49 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO