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bn:01319740n
Noun Concept
Categories: Autosomal recessive disorders, Skin conditions resulting from errors in metabolism, Lipid metabolism disorders
EN
Urbach–Wiethe disease  lipoid proteinosis  Bilateral intracranial sickle-shaped calcification of the temporal lobes  Bilateral intracranial sickle-shaped calcifications of the temporal lobes  Hyalinosis Cutis Et Mucosae
EN
Urbach–Wiethe disease is a very rare recessive genetic disorder, with approximately 400 reported cases since its discovery. Wikipedia
Definitions
Relations
Sources
EN
Urbach–Wiethe disease is a very rare recessive genetic disorder, with approximately 400 reported cases since its discovery. Wikipedia
Rare recessive genetic disorder Wikidata
IS A
rare disease
dyslipidemia
hoarseness
GENETIC ASSOCIATION
Extracellular matrix protein 1
HEALTH SPECIALTY
endocrinology
NAMED AFTER
Erich Urbach
Camillo Wiethe
Wikipedia
EN
Urbach–Wiethe disease
Wikidata
EN
lipoid proteinosis
Wikipedia Redirections
EN
Bilateral intracranial sickle-shaped calcification of the temporal lobes, Bilateral intracranial sickle-shaped calcifications of the temporal lobes, Hyalinosis cutis et mucosae, lipoid proteinosis, Lipoid proteinosis of Urbach and Wiethe, Urbach-Wieth disease, Urbach-Wiethe, Urbach-Wiethe disease, Urbach-wiethe syndrome, Urbach Wiethe disease
Wikidata Alias
EN
Hyalinosis Cutis Et Mucosae, lipid proteinosis, Lipoid Proteinosis of Urbach and Wiethe, LIPOPROTEINOSIS, Urbach–Wiethe disease

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