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apolipoproteïne A-IV-amyloïdose (aandoening)
apolipoproteïne A-IV-amyloïdose
AApoAIV-amyloïdose
Apolipoprotein A-IV amyloidosis
AApoAIV (apolipoprotein A-IV) amyloidosis
A rare nonhereditary systemic amyloidosis characterized by slowly progressive renal dysfunction, increased serum creatinine, mostly normal urine analysis with no significant proteinuria and associated heart disease. Cardiac involvement presents as hypertrophic obstructive cardiomyopathy, left ventricular outflow tract obstruction, coronary artery disease and conduction system abnormalities. Histology reveals medullar amyloid deposits, renal tubular atrophy, interstitial fibrosis, and glomerular sclerosis.
Id1187124004
StatusPrimitive
Associated morphologydepositie van amyloïd
Causative agentApolipoprotein A-IV
Finding sitestructuur van nier
SNOMED CT to Orphanet simple map439232
SNOMED CT to ICD-10 extended map
TargetE85.8
RuleTRUE
AdviceALWAYS E85.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified