familial visceral amyloidosis
ICD-10: E85.0MeSH: C538249ORPHA: 85450
Overview
type of amyloidosis that mostly affects the kidney
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with familial visceral amyloidosis, sourced from HPO and Orphanet clinical annotations.
ProteinuriaNephropathyRenal interstitial amyloid depositsRenal insufficiencyHypertensionTubulointerstitial nephritisElevated circulating creatinine concentrationAbnormality of the gastrointestinal tractDecreased glomerular filtration rateAbnormal urinary electrolyte concentrationNocturiaRenal tubular atrophyNephrotic syndromePetechiaePurpuraDecreased liver functionHepatosplenomegalyCongestive heart failureWeight lossAnemiaVomitingDiarrheaNauseaGastroesophageal refluxAbdominal painGastrointestinal hemorrhageHepatomegalyLymphadenopathyAbnormal lymph node morphologyMyopathyDecreased HDL cholesterol concentrationElevated erythrocyte sedimentation rateIntestinal obstructionTubulointerstitial fibrosisPeripheral neuropathyIntestinal perforationDecreased circulating apolipoprotein A-I concentrationDyspepsiaAbnormal testis morphologyHypogonadismOligozoospermiaMale infertilityPrimary testicular failure
Classification & Codes
ICD-10 Code
E85.0MeSH Code
C538249Orphanet Code
ORPHA:85450familial visceral amyloidosis
| ICD-10 | E85.0 |
| MeSH | C538249 |
| Orphanet | ORPHA:85450 |
| Treatments | 0 drug(s) |
| Symptoms on record | 43 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO