LD2F.10

ICD-11 MMS 2026-01

Prune belly syndrome

Description

A syndrome is characterised by cryptorchidism, urinary tract defects, and poor development of the abdominal muscles causing the skin on the abdomen to wrinkle.

Index terms

  • Prune belly syndrome
  • Eagle-Barrett syndrome
  • Obrinsky syndrome
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  • abdomen muscle deficiency syndrome
  • abdomen muscular deficiency syndrome
  • abdominal muscle aplasia syndrome
  • abdominal muscle deficiency syndrome
  • abdominal muscular deficiency syndrome
  • triad syndrome
  • Prune belly syndrome, complete form
  • Prune belly syndrome, partial form

Exclusions from above levels

  • http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Sibling codes

  • LD2F.11 – VATER association
  • LD2F.12 – Sirenomelia
  • LD2F.13 – Meckel-Gruber syndrome
  • LD2F.14 – MURCS association
  • LD2F.15 – Noonan syndrome
  • LD2F.16 – Otomandibular dysplasia
  • LD2F.1Y – Other specified syndromes with multiple structural anomalies, not of environmental origin
  • LD2F.1Z – Syndromes with multiple structural anomalies, not of environmental origin, unspecified

Foundation entity

Prune belly syndrome – http://id.who.int/icd/entity/1393408621

Part of: LD2F.1: Syndromes with multiple structural anomalies, not of environmental origin › LD2F: Syndromes with multiple structural anomalies, without predominant body system involvement › 20: Developmental anomalies