Acute metabolic disorder
Digestive system hereditary disorder
Familial disease
Hepatorenal syndrome
Hereditary nephropathy
Inherited arthrogryposis
Inherited disorder of bilirubin metabolism
Metabolic renal disease
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Familial arthrogryposis-cholestatic hepatorenal syndrome (disorder)
Familial arthrogryposis-cholestatic hepatorenal syndrome
Familial arthrogryposis - cholestatic hepatorenal syndrome
Lethal familial cholestatic AND pigmentary liver disease
familiair artrogrypose-cholestatisch hepatorenaal syndroom
familiaal artrogrypose-cholestatisch hepatorenaal syndroom
Id62216007
StatusPrimitive
Finding siteKidney structure
Finding siteLiver structure
Clinical courseSudden onset AND/OR short duration
Associated morphologyContracture
Finding siteStructure of joint region
OccurrenceCongenital
Pathological processPathological developmental process
Has interpretationImpaired
InterpretsMeasurement of renal function
Has interpretationDecreased
InterpretsRange of joint movement
ICD-10 complex map reference set
TargetQ68.8
RuleTRUE
AdviceALWAYS Q68.8
CorrelationSNOMED CT source code to target map code correlation not specified