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bn:03376544n
Noun Concept
Categories: Skin conditions resulting from errors in metabolism, Autosomal recessive disorders, Membrane transport protein disorders, Lipid metabolism disorders, Rare diseases
EN
Tangier disease  A-alphalipoprotein Neuropathy  Alpha High Density Lipoprotein Deficiency Disease  Analphalipoproteinemia  ATP-binding cassette transporter A1 deficiency
EN
Tangier disease or hypoalphalipoproteinemia is an extremely rare inherited disorder characterized by a severe reduction in the amount of high density lipoprotein, often referred to as "good cholesterol", in the bloodstream. Wikipedia
Definitions
Relations
Sources
EN
Tangier disease or hypoalphalipoproteinemia is an extremely rare inherited disorder characterized by a severe reduction in the amount of high density lipoprotein, often referred to as "good cholesterol", in the bloodstream. Wikipedia
Extremely rare inherited human disorder Wikidata
IS A
rare disease
hypolipoproteinemia
hypoalphalipoproteinemia
neurometabolic disease
GENETIC ASSOCIATION
ABCA1
APOA1
HEALTH SPECIALTY
endocrinology
NAMED AFTER
Tangier, Virginia
Wikipedia
EN
Tangier disease
Wikidata
EN
Tangier disease
Wikipedia Redirections
EN
A-alphalipoprotein Neuropathy, Alpha High Density Lipoprotein Deficiency Disease, Analphalipoproteinemia, Cholesterol thesaurismosis, Familial alpha-lipoprotein deficiency, Familial High Density Lipoprotein Deficiency Disease, Familial Hypoalphalipoproteinemia, Familial lipoprotein deficiency, HDL Lipoprotein Deficiency Disease, Tangier's disease, Tangier Disease Neuropathy, Tangier Hereditary Neuropathy, Tangler disease
Wikidata Alias
EN
Analphalipoproteinemia, ATP-binding cassette transporter A1 deficiency, Defective adenosine triphosphate-binding cassette transporter A1, familial alpha-lipoprotein deficiency, familial high density lipoprotein deficiency, familial hypoalphalipoproteinemia, High Density Lipoprotein Deficiency, Tangier Type, High Density Lipoprotein Deficiency, Type 1, TANGIER DISEASE, TANGIER DISEASE; TGD, TGD

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