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bn:03449771n
Noun Concept
SYL
No term available
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
Relations
Sources
IS A
EN
genetic disease
EN
rare disease
EN
hypertrophic cardiomyopathy
EN
sphingolipidosis
GENETIC ASSOCIATION
EN
galactosidase alpha
HEALTH SPECIALTY
EN
endocrinology
NAMED AFTER
EN
Johannes Fabry
POSSIBLE TREATMENT
EN
enzyme replacement therapy
SYMPTOMS
EN
dizziness
EN
fatigue
EN
high blood pressure
EN
renal failure
EN
nausea
+6 relations

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