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bn:03393235n
Noun Concept
SYL
No term available
EN
The GM2 gangliosidoses are a group of three related genetic disorders that result from a deficiency of the enzyme beta-hexosaminidase. Wikipedia
Relations
Sources
IS A
EN
gangliosidosis
HAS KIND
EN
Tay-Sachs disease
EN
Sandhoff disease
EN
GM2-gangliosidosis, AB variant
HEALTH SPECIALTY
EN
endocrinology

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