inherited metabolic disorder +

aceruloplasminemia
amino acid metabolic disorder +
aromatic L-amino acid decarboxylase deficiency
bilirubin metabolic disorder +
carbohydrate metabolic disorder +
cerebral amyloid angiopathy +
D-glyceric aciduria
dopamine beta-hydroxylase deficiency
familial hypocalciuric hypercalcemia +
familial visceral amyloidosis
glycerol kinase deficiency
Gordon Holmes syndrome
Greenberg dysplasia
HRPT-related hyperuricemia
hyperphosphatemic familial tumoral calcinosis
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 +
poor metabolism of thiopurines +
porphyria +
primary cutaneous amyloidosis +
purine-pyrimidine metabolic disorder +
pyrimidine metabolic disorder +
transthyretin amyloidosis
trimethylaminuria
variant ABeta2M amyloidosis
warfarin resistance
warfarin sensitivity
X-linked warfarin sensitivity

cerebral folate receptor alpha deficiency
familial isolated deficiency of vitamin E
glutamate formiminotransferase deficiency
hereditary folate malabsorption
pyridoxamine 5'-phosphate oxidase deficiency
vitamin B12 deficiency +