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
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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