Congenital anomaly of skeletal bone
Congenital anomaly of skin
Congenital anomaly of skin
Congenital connective tissue disorder
Connective tissue hereditary disorder
Developmental hereditary disorder
Hereditary disorder of musculoskeletal system
Hereditary disorder of the integument
Hereditary metabolic disease
Metabolic bone disease
Metabolic bone disease
Metabolic disease of collagen
Metabolic disease of collagen
Musculoskeletal and connective tissue disorder
Skeletal dysplasia
Skin lesion
Skin lesion
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Ehlers-Danlos syndrome (disorder)
Ehlers-Danlos syndrome
Dystrophia mesodermalis congenita
Cutis hyperelastica
Meekeren-Ehlers-Danlos syndrome
Fibrodysplasia elastica generalisata
Danlos disease
Cutis elastica
Hereditary collagen dysplasia
India rubber skin
Cutis hyperelastica dermatorrhexis
Dermatorrhexis with dermatochalasis AND arthrochalasis
Ehlers-Danlos-syndroom
cutis hyperelastica
EDS
syndroom van Ehlers-Danlos
syndroom van Ehlers-Danlos
Erfelijke aandoening met als belangrijkste kenmerken een zeer rekbare huid, overstrekbare gewrichten, met als mogelijk gevolg het sneller ontstaan van slijtage van de gewrichten en het vaker optreden van blauwe plekken.
Id398114001
StatusPrimitive
Associated morphologyMorphologically abnormal structure
Finding siteConnective tissue structure
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyDysplasia
Finding siteSkin structure
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyDysplasia
Finding siteBone structure
Finding siteBone structure
OccurrenceCongenital
OccurrenceCongenital
Pathological processPathological developmental process
PALGA thesaurus simple reference set for pathology
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ79.6
RuleTRUE
AdviceALWAYS Q79.6
CorrelationSNOMED CT source code to target map code correlation not specified
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Brittle cornea syndrome
Ehlers-Danlos and osteogenesis imperfecta syndrome
Ehlers-Danlos syndrome cardiac valvular type
Ehlers-Danlos syndrome classic type2
Ehlers-Danlos syndrome due to tenascin-X deficiency
Ehlers-Danlos syndrome kyphoscoliotic type2
Ehlers-Danlos syndrome musculocontractural type
Ehlers-Danlos syndrome progeroid type
Ehlers-Danlos syndrome spondylocheirodysplastic type
Ehlers-Danlos syndrome, dysfibronectinemic
Ehlers-Danlos syndrome, familial joint laxity type
Ehlers-Danlos syndrome, non hydroxylysine deficient ocular type
Ehlers-Danlos syndrome, procollagen proteinase deficient
Ehlers-Danlos syndrome, procollagen proteinase resistant
Ehlers-Danlos syndrome, type 3
Ehlers-Danlos syndrome, type 4
Ehlers-Danlos syndrome, type 5
Ehlers-Danlos syndrome, type 8
Pre-existing Ehlers-Danlos syndrome during pregnancy