LD28.1Y Other specified types of Ehlers-Danlos syndrome
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
postcoordination
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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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