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bn:03449771n
Noun Concept
Categories: Rare diseases, Articles with short description, Cardiogenetic disorders, Lysosomal storage diseases, Skin conditions resulting from errors in metabolism
EN
Fabry disease  Fabry's disease  alpha-galactosidase A deficiency  alpha galactosidase deficiency  Anderson-Fabry's Disease
EN
Fabry disease, also known as Anderson–Fabry disease, is a rare genetic disease that can affect many parts of the body, including the kidneys, heart, and skin. Wikipedia
Definitions
Relations
Sources
EN
Fabry disease, also known as Anderson–Fabry disease, is a rare genetic disease that can affect many parts of the body, including the kidneys, heart, and skin. Wikipedia
Rare human genetic lysosomal storage disorder Wikidata
IS A
genetic disease
rare disease
hypertrophic cardiomyopathy
sphingolipidosis
GENETIC ASSOCIATION
galactosidase alpha
HEALTH SPECIALTY
endocrinology
NAMED AFTER
Johannes Fabry
POSSIBLE TREATMENT
enzyme replacement therapy
SYMPTOMS
dizziness
fatigue
high blood pressure
renal failure
nausea
+6 relations
Wikipedia
EN
Fabry disease
Wikidata
EN
Fabry disease
Wikipedia Redirections
EN
alpha-galactosidase A deficiency, Anderson-Fabry's Disease, Anderson-Fabry disease, Anderson–Fabry disease, Angiokeratoma Corporis Diffusum, Angiokeratoma corporis diffusum, Angiokeratoma corporis diffusum of Fabry, Angiokeratoma corporis diffusum universale, Angiokeratoma diffuse, Anglokeratoma corporis diffusum universale, Ceramide trihexosidase deficiency, Ceramide trihexosidosis, Diffuse angiokeratoma, Diffuse angiokeratosis, Diffuse anglokeratoma, Fabray's disease, Fabrey's disease, Fabry's disease, Fabrys disease, GLA (gene)
Wikidata Alias
EN
alpha-galactosidase A deficiency, alpha galactosidase deficiency, Anderson-Fabry disease, angiokeratoma corporis diffusum, Ceramide Trihexosidase Deficiency, deficiency of melibiase, Diffuse angiokeratoma, Fabry's disease, FABRY DISEASE, Fabry Disease, Cardiac Variant, FD, Gla Deficiency, Hereditary Dystopic Lipidosis

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