DA42.6

ICD-11 MMS 2026-01

Menetrier disease

Description

Gastritis characterised by gastric mucosal hypertrophy, which may cause the giant rugal folds. The thickening of the rugae is predominantly caused by the expansion of the epithelial cell compartment of the gastric mucosa. Patients with Ménétrier disease most often present with hypoalbuminemia secondary to a loss of albumin into the gastric lumen.

Index terms

  • Menetrier disease
  • Giant hypertrophic gastritis
  • Giant hypertrophic hypersecretory gastritis

Exclusions from above levels

  • DD50.0 – Diaphragmatic hernia
  • DE12.1 – Gastrostomy malfunction
  • 01 – Certain infectious or parasitic diseases
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  • 02 – Neoplasms
  • 05 – Endocrine, nutritional or metabolic diseases
  • 06 – Mental, behavioural or neurodevelopmental disorders
  • 18 – Complications of pregnancy, childbirth and the puerperium
  • 22 – Injury, poisoning or certain other consequences of external causes

Sibling codes

  • DA42.0 – Autoimmune gastritis
  • DA42.1 – Helicobacter pylori induced gastritis
  • DA42.2 – Eosinophilic gastritis
  • DA42.3 – Lymphocytic gastritis
  • DA42.4 – Allergic gastritis
  • DA42.5 – Gastritis due to duodenogastric reflux
  • DA42.7 – Gastritis of unknown aetiology with specific endoscopic or pathological features
  • DA42.8 – Gastritis due to external causes
  • DA42.9 – Gastric phlegmon
  • DA42.Y – Other specified gastritis
  • DA42.Z – Gastritis, unspecified

Foundation entity

Menetrier disease – http://id.who.int/icd/entity/1343994188

Allowed postcoordination axes

Part of: DA42: Gastritis › 13: Diseases of the digestive system