LD2B

ICD-11 MMS 2026-01

Syndromes with premature ageing appearance as a major feature

Description

A heterogeneous group of hereditary syndromes in which affected individuals do or appear to age at an accelerated rate.

Index terms

  • Syndromes with premature ageing appearance as a major feature
  • Progeroid syndromes
  • premature aging syndrome
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  • progeria syndrome
  • Cockayne syndrome
  • Cockayne syndrome type 1
  • Cockayne syndrome type 2
  • Cockayne syndrome type 3
  • Xeroderma pigmentosum-Cockayne syndrome complex
  • Cerebro-oculo-facio-skeletal syndrome
  • COFS - [Cerebro-oculo-facio-skeletal syndrome]
  • COFS - [Cerebrooculofacioskeletal syndrome]
  • Cerebrooculofacioskeletal syndrome
  • Pena-Shokeir syndrome type 2
  • Rothmund-Thomson syndrome
  • Poikiloderma congenitale
  • Poikiloderma of Rothmund-Thomson
  • Rothmund-Thomson syndrome type 1
  • Rothmund-Thomson syndrome type 2
  • Progeria
  • Gilford-Hutchinson syndrome
  • Hutchinson-Gilford syndrome
  • Werner syndrome
  • Pangeria
  • Atypical Werner syndrome
  • Acrogeria
  • Gottron syndrome
  • Wiedemann-Rautenstrauch progeroid syndrome
  • Neonatal progeroid syndrome
  • Mulvihill-Smith progeroid syndrome
  • Geroderma osteodysplasticum
  • Wrinkly skin syndrome
  • Metageria
  • Hallermann-Streiff-François syndrome
  • Kindler syndrome
  • Bullous acrokeratotic poikiloderma of Kindler and Weary
  • Congenital poikiloderma with bullae and progressive cutaneous atrophy
  • Hereditary acrokeratotic poikiloderma
  • Weary–Kindler syndrome

Inclusions

  • Progeroid syndromes
  • Cockayne syndrome
  • Rothmund-Thomson syndrome
  • Progeria
  • Kindler syndrome

Excludes

Exclusions from above levels

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

Sibling codes

  • LD20 – Syndromes with central nervous system anomalies as a major feature
  • LD21 – Syndromes with eye anomalies as a major feature
  • LD22 – Syndromes with dental anomalies as a major feature
  • LD23 – Syndromes with vascular anomalies as a major feature
  • LD24 – Syndromes with skeletal anomalies as a major feature
  • LD25 – Syndromes with face or limb anomalies as a major feature
  • LD26 – Syndromes with limb anomalies as a major feature
  • LD27 – Syndromes with skin or mucosal anomalies as a major feature
  • LD28 – Syndromes with connective tissue involvement as a major feature
  • LD29 – Syndromes with obesity as a major feature
  • LD2A – Malformative disorders of sex development
  • LD2C – Overgrowth syndromes
  • LD2D – Phakomatoses or hamartoneoplastic syndromes
  • LD2E – Syndromes with structural anomalies due to inborn errors of metabolism
  • LD2F – Syndromes with multiple structural anomalies, without predominant body system involvement
  • LD2G – Conjoined twins
  • LD2H – Syndromic genetic deafness
  • LD2Y – Other specified multiple developmental anomalies or syndromes
  • LD2Z – Multiple developmental anomalies or syndromes, unspecified

Foundation entity

Syndromes with premature ageing appearance as a major feature – http://id.who.int/icd/entity/1520135105

Part of: 20: Developmental anomalies