Autosomal dominant hereditary disorder
Autosomal dominant hereditary disorder
Developmental hereditary disorder
Dysplasia with defective mineralization
Dysplasia with defective mineralization
Hereditary disorder of musculoskeletal system
Hereditary disorder of musculoskeletal system
Hereditary metabolic disease
Hypophosphatemia
Hypophosphatemia
Lesion of bone
Metabolic bone disease
Metabolic bone disease
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Autosomal dominant hypophosphatemic bone disease (disorder)
Autosomal dominant hypophosphatemic bone disease
autosomaal dominante hypofosfatemische botziekte
Id237890006
StatusDefined
Associated morphologyDysplasia
Finding siteOsteoid tissue
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyImpaired mineralization
Finding siteBone structure
OccurrenceCongenital
Pathological processPathological developmental process
Due toSpecific renal tubule transport defect
ICD-10 complex map reference set
TargetE83.3
RuleTRUE
AdviceALWAYS E83.3
CorrelationSNOMED CT source code to target map code correlation not specified
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Autosomal dominant hypophosphatemic rickets
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis