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LD28.1Y Other specified types of Ehlers-Danlos syndrome

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

postcoordination

synonyms

• Other specified types of Ehlers-Danlos syndrome
• Ehlers-Danlos syndrome, hypermobile type
• Familial ligamentous laxity
• Benign joint hypermobility syndrome
• Ehlers-Danlos syndrome type 3
• Ehlers-Danlos syndrome, vascular type
• Sack-Barabas syndrome
• Ehlers-Danlos syndrome type 4
• Ehlers-Danlos syndrome, rare variants
• Ehlers-Danlos syndrome, X-linked
• Ehlers-Danlos syndrome type 5
• Ehlers-Danlos syndrome, kyphoscoliotic type
• Ehlers-Danlos syndrome type 6
• Ehlers-Danlos syndrome type 6A
• Ehlers-Danlos syndrome type 6B
• Brittle cornea syndrome
• Ehlers-Danlos syndrome, arthrochalasic type
• Ehlers-Danlos syndrome type 7
• Ehlers-Danlos syndrome type 7A
• Ehlers-Danlos syndrome type 7B
• Ehlers-Danlos syndrome, dermatosparaxis type
• Ehlers-Danlos syndrome type 7C
• Ehlers-Danlos syndrome, progeroid type
• Galactosyltransferase I deficiency
• Xylosylprotein 4-beta-galactosyltransferase deficiency
• Defective biosynthesis of proteodermatan sulphate
• Ehlers-Danlos syndrome, cardiac valvular type
• Ehlers-Danlos syndrome, classic-like type
• Ehlers-Danlos syndrome with periventricular heterotopia
• Ehlers-Danlos-osteogenesis imperfecta syndrome
• Ehlers-Danlos syndrome, spondylocheirodysplastic type
• Ehlers-Danlos syndrome due to tenascin-X deficiency
• Ehlers-Danlos syndrome, periodontitis type
• Ehlers-Danlos syndrome type 8
• Ehlers-Danlos syndrome, vascular-like type
• Ehlers-Danlos syndrome, dysfibronectinaemic type
• Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormality
• Ehlers-Danlos syndrome, fibronectin-deficient
• Ehlers-Danlos syndrome type 10
• Other specified Ehlers-Danlos syndrome variant
• Ehlers-Danlos syndrome of undetermined or unspecified type
• Ehlers-Danlos syndrome NOS

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