- Congenital anomaly of skin (disorder)
- Connective tissue hereditary disorder (disorder)
- Hereditary disorder of musculoskeletal system
- Hereditary disorder of the integument
- Metabolic bone disease (disorder)
- Metabolic disease of collagen (disorder)
- Skeletal dysplasia
- Skin lesion
Name: Ehlers-Danlos syndrome
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- Ehlers-Danlos syndrome (disorder)
- Ehlers-Danlos syndrome
- Cutis hyperelastica dermatorrhexis
- Dystrophia mesodermalis congenita
- India rubber skin
- Dermatorrhexis with dermatochalasis AND arthrochalasis
- Hereditary collagen dysplasia
- Meekeren-Ehlers-Danlos syndrome
- Cutis elastica
- Cutis hyperelastica
- Danlos disease
- Fibrodysplasia elastica generalisata
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Concept ID: 398114001- Ehlers-Danlos syndrome
- Cutis hyperelastica dermatorrhexis
- Dystrophia mesodermalis congenita
- India rubber skin
- Dermatorrhexis with dermatochalasis AND arthrochalasis
- Hereditary collagen dysplasia
- Meekeren-Ehlers-Danlos syndrome
- Cutis elastica
- Cutis hyperelastica
- Danlos disease
- Fibrodysplasia elastica generalisata
Hide descriptions.
Read Codes: PGy2. X50Cz
ICD-10 Codes: Q796
- Brittle cornea syndrome
- Cutis laxa, x-linked
- Ehlers-Danlos and osteogenesis imperfecta syndrome (disorder)
- Ehlers-Danlos syndrome cardiac valvular type
- + Ehlers-Danlos syndrome classic type (disorder)
- Ehlers-Danlos syndrome kyphoscoliotic and deafness type
- Ehlers-Danlos syndrome kyphoscoliotic type (disorder)
- Ehlers-Danlos syndrome musculocontractural type
- Ehlers-Danlos syndrome progeroid type
- Ehlers-Danlos syndrome vascular-like type
- Ehlers-Danlos syndrome with periventricular heterotopia
- Ehlers-Danlos syndrome, dysfibronectinaemic
- Ehlers-Danlos syndrome, familial joint laxity type
- + Ehlers-Danlos syndrome, hydroxylysine-deficient (disorder)
- Ehlers-Danlos syndrome, non hydroxylysine deficient ocular type (disorder)
- Ehlers-Danlos syndrome, procollagen proteinase deficient (disorder)
- Ehlers-Danlos syndrome, procollagen proteinase resistant (disorder)
- Ehlers-Danlos syndrome, type 3
- + Ehlers-Danlos syndrome, type 4
- Ehlers-Danlos syndrome, type 5
- Ehlers-Danlos syndrome, type 8 (disorder)