LD28.2 Genetically-determined cutis laxa

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

synonyms

• Genetically-determined cutis laxa
• Autosomal recessive cutis laxa
• Autosomal recessive cutis laxa, type 1
• Autosomal recessive cutis laxa with severe systemic involvement
• Autosomal recessive cutis laxa, pulmonary emphysema type
• ARCL-1 - [Autosomal recessive cutis laxa, type 1] (MIM 219100)
• Autosomal recessive cutis laxa, type 2A
• Autosomal recessive cutis laxa, Debré type
• ARCL-2A - [Autosomal recessive cutis laxa, type 2A] (MIM 219200)
• Autosomal recessive cutis laxa, type 2B
• Cutis laxa with bone dystrophy
• Cutis laxa with joint laxity and developmental delay
• ARCL-2B - [Autosomal recessive cutis laxa, type 2B] (MIM 612940)
• Autosomal recessive cutis laxa, type 3
• Cutis laxa - corneal clouding - intellectual deficit
• Progeroid syndrome, De Barsy type
• De Barsy syndrome
• ARCL-3 - [Autosomal recessive cutis laxa, type 3] (MIM 219150)
• Autosomal dominant cutis laxa
• ADCL - [Autosomal dominant cutis laxa] (MIM 123700)
• Syndromic cutis laxa
• Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
• Urban-Rifkin-Davis syndrome
• URDS - [Urban-Rifkin-Davis syndrome] (MIM 613177)
• X-linked cutis laxa
• Ehlers-Danlos syndrome type IX
• Occipital horn syndrome
• OHS - [occipital horn syndrome]
• Cutis laxa - Marfanoid syndrome
• Macrocephaly – alopecia – cutis laxa – scoliosis syndrome
• MACS syndrome (MIM 613075)
• MACS - [Macrocephaly – alopecia – cutis laxa – scoliosis syndrome]
• SCARF syndrome
• Skeletal abnormalities – Cutis laxa – craniostenosis – Ambiguous genitalia – psychomotor Retardation and Facial abnormalities

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