inherited metabolic disorder +
amyloidosis +

aceruloplasminemia
amino acid metabolic disorder +
apolipoprotein A-IV associated amyloidosis
aromatic L-amino acid decarboxylase deficiency
bilirubin metabolic disorder +
carbohydrate metabolic disorder +
D-glyceric aciduria
dialysis-related amyloidosis
dopamine beta-hydroxylase deficiency
familial hypocalciuric hypercalcemia +
familial visceral amyloidosis
familial visceral amyloidosis
glycerol kinase deficiency
Gordon Holmes syndrome
Greenberg dysplasia
HRPT-related hyperuricemia
hyperphosphatemic familial tumoral calcinosis
immunoglobulin heavy chain amyloidosis
immunoglobulin heavy-and-light chain
immunoglobulin light chain amyloidosis
immunoglobulin light chain amyloidosis
isolated elevated serum creatine phosphokinase levels
isolated sulfite oxidase deficiency
lipid metabolism disorder +
lysosomal storage disease +
metal metabolism disorder +
mitochondrial metabolism disease +
multiple acyl-CoA dehydrogenase deficiency
peroxisomal disease +
phosphoribosylpyrophosphate synthetase superactivity
plasma protein metabolism disease +
porphyria +
primary cutaneous amyloidosis +
primary cutaneous amyloidosis +
purine-pyrimidine metabolic disorder +
pyrimidine metabolic disorder +
serum amyloid A amyloidosis
thiopurine S-methyltransferase deficiency
transthyretin amyloidosis
transthyretin amyloidosis
trimethylaminuria
variant ABeta2M amyloidosis
variant ABeta2M amyloidosis
vitamin metabolic disorder +
warfarin resistance
warfarin sensitivity
wild-type amyloidosis
X-linked warfarin sensitivity

APP-related cerebral amyloid angiopathy
CST3-related cerebral amyloid angiopathy
ITM2B-related cerebral amyloid angiopathy 1
ITM2B-related cerebral amyloid angiopathy 2