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bn:01873314n
Noun Concept
SYL
No term available
EN
GM2-gangliosidosis, AB variant is a rare, autosomal recessive metabolic disorder that causes progressive destruction of nerve cells in the brain and spinal cord. Wikipedia
Relations
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IS A
EN
rare disease
EN
GM2 gangliosidosis
GENETIC ASSOCIATION
EN
GM2A
HEALTH SPECIALTY
EN
neurology
EN
endocrinology
EN
medical genetics

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