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Xanthoma
Xanthoma
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Skin conditions resulting from errors in metabolism
(86)
Apolipoprotein B deficiency
Combined hyperlipidemia
Lipoid proteinosis
Lipoprotein lipase deficiency
Tangier disease
Tangier disease
X-linked adrenoleuk- odystrophy
Xanthelasma
Xanthoma tuberosum
Xanthomatosis
Acute intermittent porphyria
Alkaptonuria
Amyloid purpura
Amyloidosis
B-mannosidase deficiency
CADASIL syndrome
Calcinosis cutis
Carotenosis
Cerebrotendineous xanthomatosis
Citrullinemia
Diabetic bulla
Diabetic cheiroarthropathy
Diabetic dermadrome
Diabetic dermopathy
Dystrophic calcinosis cutis
Eruptive xanthoma
Erythropoietic porphyria
Erythropoietic protoporphyria
Fabry disease
Familial apoprotein CII deficiency
Familial dysbetalip- oproteinemia
Familial hypertrigl- yceridemia
Farber disease
Fucosidosis
Gaucher's disease
Gout
Gunther disease
Hartnup disease
Hepatoeryt- hropoietic porphyria
Hereditary coproporphyria
Heredofamilial amyloidosis
Hunter syndrome
Hurler syndrome
Hyaluronidase deficiency
Iatrogenic calcinosis cutis
Idiopathic scrotal calcinosis
Lafora disease
Lesch–Nyhan syndrome
Lichen amyloidosis
Limited joint mobility
Macular amyloidosis
Medication-induced hyperlipop- roteinemia
Metastatic calcinosis cutis
Morquio syndrome
Myxedema
Necrobiosis lipoidica
Niemann–Pick disease
Nodular amyloidosis
Nodular xanthoma
Normolipop- roteinemic xanthomatosis
Ochronosis
Osteoma cutis
Palmar xanthoma
Phenylketonuria
Porphyria
Porphyria cutanea tarda
Primary cutaneous amyloidosis
Primary systemic amyloidosis
Prolidase deficiency
Pseudoporphyria
Secondary cutaneous amyloidosis
Secondary systemic amyloidosis
Sialidosis
Sitosterolemia
Subepidermal calcified nodule
Transient erythroporphyria of infancy
Traumatic calcinosis cutis
Tuberoeruptive xanthoma
Tumoral calcinosis
Variegate porphyria
Verruciform xanthoma
Waxy skin
Xanthoma diabeticorum
Xanthoma planum
Xanthoma striatum palmare
Xanthoma tendinosum
Xanthomatous biliary cirrhosis
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Hepatology
Primary biliary cirrhosis
Hepatolenticular degeneration
Fatty liver
Xanthelasma
Symptoms
Xerostomia
Skin lesion
Diseases and disorders
(35)
Xanthoma disseminatum
Adrenoleuk- odystrophy x-linked
Xeroderma pigmentosa
Agammaglobulinemia
X linked agammaglobulinemia
X linked agammaglobulinemia
Xerophthalmia
Xanthosis
Malonic aciduria
Xanthinuria
Mitochondrial trifunctional protein deficiency
Lecithin cholesterol acyltransferase deficiency
Thalessemia
Hyperlipop- roteinemia
Adiposis dolorosa
Hypolipoproteinemia
Lichen planus
Histiocytes
Abetalipop- roteinemia
Xanthogranulomatous pyelonephritis
Aphthous ulcer
Metabolic disorders
X-linked retinoschisis
Mucous colitis
Nodule (medicine)
Regional enteritis
Osgood Schlatter disease
Osteochondrosis
Parotitis
Brittle bone disease
Lipoprotein lipase deficiency
Primary biliary cirrhosis
Xerostomia
Tangier disease
Hepatolenticular degeneration
Fatty liver
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Autosomal recessive disorders
(9)
Xeroderma pigmentosa
Lipoid proteinosis
Malonic aciduria
Mitochondrial trifunctional protein deficiency
Lecithin cholesterol acyltransferase deficiency
Lecithin cholesterol acyltransferase deficiency
Thalessemia
Abetalipop- roteinemia
Tangier disease
Hepatolenticular degeneration
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Gastroenterology
Hypochlorhydria
Xanthelasma
Primary biliary cirrhosis
Mucous colitis
Hepatolenticular degeneration
Regional enteritis
Genetic disorders
(16)
Xanthism
Barraquer-Simons Syndrome
Hypoalphal- ipoproteinemia
X-linked dominant
Genetic condition
Genetic condition
X-linked adrenoleuk- odystrophy
Malonic aciduria
Xanthinuria
Mitochondrial trifunctional protein deficiency
Lecithin cholesterol acyltransferase deficiency
Thalessemia
Abetalipop- roteinemia
Tangier disease
Hepatolenticular degeneration
Regional enteritis
Brittle bone disease
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Dermatologic terminology
Xerosis
Papules
Xerostomia
Skin lesion
Lipid disorders
(15)
Blood lipids
Familial hyperchole- sterolemia
Hyperchole- sterolemia
Cholesterol
Cholesterol Depletion
Cholesterol Depletion
Combined hyperlipidemia
High-density lipoprotein
Hyperlipop- roteinemia
Hypertrigl- yceridemia
Hypocholesterolemia
Lipoprotein lipase deficiency
Lipoprotein(a)
Low-density lipoprotein
Mevalonate inhibition
Triglyceride
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Mononuclear phagocytes
Macrophages
Dendritic cell
Histiocytes
Langerhans cell
Monocyte
Splenocyte
Medicine
Hypobetali- poproteinemia
Xanthochromia
Xanthopsia
Xerogram
Diseases and disorders
Hypolipoproteinemia
Organic compounds
Xanthogenate
Xanthene
Xylulose
Xanthine
See also
(20)
Xalatan
Xanthine
Xanthochroi
Xanthogranuloma, juvenile
Xanthidium
Xanthidium
Xanthorhiza
Liver abcess
Xylose
Veneral diseases
Xanthopterin
Xanthophyceae
Xeromammography
Xantusiidae
Biopsy
Cancer
Diabetes
X rays
Xanthorrhoeaceae
Levator palpebrae superioris muscle
LIPD
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