[{"n": "Amyloidosis", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/amyloidosis/", "s": "A group of protein misfolding diseases causing amyloid buildup in tissues."}, {"n": "Anderson–Fabry disease", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/anderson-fabry-disease/", "s": "A rare X-linked lysosomal storage disease with multisystem involvement."}, {"n": "Angiokeratoma corporis diffusum", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/angiokeratoma-corporis-diffusum/", "s": "A rare X-linked lysosomal storage disease with multisystem involvement."}, {"n": "Broad beta disease", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/broad-beta-disease/", "s": "A lipid disorder causing palm xanthomas and early heart disease."}, {"n": "Calcinosis cutis", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/calcinosis-cutis/", "s": "Calcium deposits in skin and subcutaneous tissue, with five recognized types."}, {"n": "Carotenoderma", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/carotenoderma/", "s": "Orange skin discoloration from excess dietary carotenoids, harmless and reversible."}, {"n": "Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy syndrome", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/cerebral-autosomal-dominant-arteriopathy-with-subcortical-infarcts-and-leukoencephalopathy-syndrome/", "s": "Most common hereditary stroke disorder from NOTCH3 mutations."}, {"n": "Cerebrotendinous xanthomatosis", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/cerebrotendinous-xanthomatosis/", "s": "Rare bile acid disorder causing neurological issues, cataracts, and tendon xanthomas."}, {"n": "Chylomicronemia", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/chylomicronemia/", "s": "A condition of severe hypertriglyceridemia due to defective chylomicron breakdown."}, {"n": "Chylomicronemia syndrome", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/chylomicronemia-syndrome/", "s": "Severe hypertriglyceridemia from defective chylomicron clearance."}, {"n": "Citrullinemia", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/citrullinemia/", "s": "A urea cycle disorder causing toxic ammonia buildup."}, {"n": "Congenital erythropoietic porphyria", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/congenital-erythropoietic-porphyria/", "s": "A rare porphyria causing severe photosensitivity and erythrodontia."}, {"n": "Diabetic cheiroarthropathy", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/diabetic-cheiroarthropathy/", "s": "Waxy, thickened skin and limited finger joint mobility in diabetes."}, {"n": "Doss porphyria", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/doss-porphyria/", "s": "An extremely rare hepatic porphyria from ALAD deficiency."}, {"n": "Erythropoietic porphyria", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/erythropoietic-porphyria/", "s": "A porphyria with enzyme deficiency in red blood cells."}, {"n": "Erythropoietic protoporphyria", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/erythropoietic-protoporphyria/", "s": "A painful photosensitivity disorder from defective heme synthesis."}, {"n": "Fabry disease", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/fabry-disease/", "s": "A rare X-linked lysosomal storage disease with multisystem involvement."}, {"n": "Familial alpha-lipoprotein deficiency", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/familial-alpha-lipoprotein-deficiency/", "s": "Rare disorder causing severe HDL deficiency and cholesterol buildup."}, {"n": "Familial amyloid polyneuropathy", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/familial-amyloid-polyneuropathy/", "s": "An inherited neurodegenerative disease caused by transthyretin protein misfolding."}, {"n": "Familial Amyloidosis, Finnish Type", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/familial-amyloidosis-finnish-type/", "s": "Amyloidosis from mutated plasma gelsolin, primarily in Finland."}, {"n": "Familial combined hyperlipidemia", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/familial-combined-hyperlipidemia/", "s": "A common inherited lipid disorder raising LDL and triglycerides."}, {"n": "Familial dysbetalipoproteinemia", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/familial-dysbetalipoproteinemia/", "s": "A lipid disorder causing xanthomas and early heart disease."}, {"n": "Familial hypertriglyceridemia", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/familial-hypertriglyceridemia/", "s": "A genetic disorder of elevated triglycerides due to VLDL overproduction."}, {"n": "Farber disease", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/farber-disease/", "s": "Rare lysosomal storage disease from acid ceramidase deficiency."}, {"n": "Fibrocytic dysmucopolysaccharidosis", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/fibrocytic-dysmucopolysaccharidosis/", "s": "A rare lysosomal storage disease from acid ceramidase deficiency."}, {"n": "Fucosidosis", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/fucosidosis/", "s": "A fatal lysosomal storage disorder from alpha-L-fucosidase deficiency."}, {"n": "Gargoylism", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/gargoylism/", "s": "A severe lysosomal storage disease causing early death."}, {"n": "Gaucher's disease", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/gaucher-s-disease/", "s": "A lysosomal storage disease from glucocerebroside accumulation."}, {"n": "Gunther disease", "u": "/e/skin-conditions-resulting-from-errors-in-metabolism/gunther-disease/", "s": "A rare congenital porphyria causing severe photosensitivity and hemolytic anemia."}]