LD2B Syndromes with premature ageing appearance as a major feature

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

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

inclusions

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

exclusions

• Xeroderma pigmentosum  (LD27.1)
• Cutis laxa  (EE41.0)

code elsewhere

• Ehlers-Danlos syndrome, progeroid type  (LD28.1Y)
• Autosomal recessive cutis laxa, type 3  (LD28.2)
• Bloom syndrome  (4A01.31)
• Ataxia-telangiectasia  (4A01.31)
• Mandibuloacral dysplasia  (LD27.6Z)

synonyms

• Syndromes with premature ageing appearance as a major feature
• Progeroid syndromes
• premature aging syndrome
• 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
• Pena-Shokeir syndrome type 2
• Cerebrooculofacioskeletal syndrome
• COFS - [Cerebro-oculo-facio-skeletal syndrome]
• COFS - [Cerebrooculofacioskeletal syndrome]
• Rothmund-Thomson syndrome
• Poikiloderma of Rothmund-Thomson
• Poikiloderma congenitale
• Rothmund-Thomson syndrome type 1
• Rothmund-Thomson syndrome type 2
• Progeria
• Hutchinson-Gilford syndrome
• Gilford-Hutchinson 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 (MIM 173650)

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