LD28.2

ICD-11 MMS 2026-01

Genetically-determined cutis laxa

Index terms

  • Genetically-determined cutis laxa
  • Autosomal recessive cutis laxa
  • Autosomal recessive cutis laxa, type 1
Show allHide
  • ARCL-1 - [Autosomal recessive cutis laxa, type 1] (MIM 219100)
  • Autosomal recessive cutis laxa with severe systemic involvement
  • Autosomal recessive cutis laxa, pulmonary emphysema type
  • Autosomal recessive cutis laxa, type 2A
  • ARCL-2A - [Autosomal recessive cutis laxa, type 2A] (MIM 219200)
  • Autosomal recessive cutis laxa, Debré type
  • Autosomal recessive cutis laxa, type 2B
  • ARCL-2B - [Autosomal recessive cutis laxa, type 2B] (MIM 612940)
  • Cutis laxa with bone dystrophy
  • Cutis laxa with joint laxity and developmental delay
  • Autosomal recessive cutis laxa, type 3
  • ARCL-3 - [Autosomal recessive cutis laxa, type 3] (MIM 219150)
  • Cutis laxa - corneal clouding - intellectual deficit
  • De Barsy syndrome
  • Progeroid syndrome, De Barsy type
  • Autosomal dominant cutis laxa
  • ADCL - [Autosomal dominant cutis laxa] (MIM 123700)
  • Syndromic cutis laxa
  • Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
  • URDS - [Urban-Rifkin-Davis syndrome] (MIM 613177)
  • Urban-Rifkin-Davis syndrome
  • X-linked cutis laxa
  • Ehlers-Danlos syndrome type IX
  • OHS - [occipital horn syndrome]
  • Occipital horn syndrome
  • Cutis laxa - Marfanoid syndrome
  • Macrocephaly – alopecia – cutis laxa – scoliosis syndrome
  • MACS - [Macrocephaly – alopecia – cutis laxa – scoliosis syndrome]
  • MACS syndrome
  • SCARF syndrome
  • Skeletal abnormalities – Cutis laxa – craniostenosis – Ambiguous genitalia – psychomotor Retardation and Facial abnormalities

Exclusions from above levels

  • EC40 – Pseudoxanthoma elasticum
  • EE41.0 – Cutis laxa
  • http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Sibling codes

  • LD28.0 – Marfan syndrome or Marfan-related disorders
  • LD28.1 – Ehlers-Danlos syndrome
  • LD28.Y – Other specified syndromes with connective tissue involvement as a major feature
  • LD28.Z – Syndromes with connective tissue involvement as a major feature, unspecified

Foundation entity

Genetically-determined cutis laxa – http://id.who.int/icd/entity/2024159409

Part of: LD28: Syndromes with connective tissue involvement as a major feature › 20: Developmental anomalies