CA25.0

ICD-11 MMS 2026-01

Classical cystic fibrosis

Index terms

  • Classical cystic fibrosis
  • Pulmonary manifestations of classical cystic fibrosis
  • fibrocystic lung disease
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  • Exacerbation of pulmonary manifestations of classical cystic fibrosis
  • Otorhinolaryngological manifestations of classical cystic fibrosis
  • Digestive manifestations of classical cystic fibrosis
  • meconium ileus of newborn
  • Digestive haemorrhage in classical cystic fibrosis
  • Distal ileal obstruction syndrome in classical cystic fibrosis
  • distal intestinal obstruction syndrome
  • Meconium ileus in classical cystic fibrosis
  • Meconium obstruction of intestine in mucoviscidosis
  • Meconium ileus in cystic fibrosis, with perforation
  • Hepatic manifestations of classical cystic fibrosis
  • Elevated hepatic enzymes in classical cystic fibrosis
  • Portal hypertension in classical cystic fibrosis
  • Liver cirrhosis in classical cystic fibrosis
  • Osteoporosis in classical cystic fibrosis
  • Male infertility in classical cystic fibrosis
  • Female hypofertility in classical cystic fibrosis
  • Polyneuropathy in classical cystic fibrosis

Exclusions from above levels

  • 01 – Certain infectious or parasitic diseases
  • 05 – Endocrine, nutritional or metabolic diseases
  • 18 – Complications of pregnancy, childbirth and the puerperium
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  • 19 – Certain conditions originating in the perinatal period
  • 20 – Congenital malformations, deformations and chromosomal abnormalities
  • 22 – Injury, poisoning or certain other consequences of external causes

Sibling codes

  • CA25.1 – Atypical cystic fibrosis
  • CA25.2 – Subclinical cystic fibrosis
  • CA25.Z – Cystic fibrosis, unspecified

Foundation entity

Classical cystic fibrosis – http://id.who.int/icd/entity/290257878

Allowed postcoordination axes

Part of: CA25: Cystic fibrosis › 12: Diseases of the respiratory system