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bn:01617535n
Noun Concept
NL
No term available
EN
X-linked spinal muscular atrophy type 2, also known as arthrogryposis multiplex congenita X-linked type 1, is a rare neurological disorder involving death of motor neurons in the anterior horn of spinal cord resulting in generalised muscle wasting. Wikipedia
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IS A
ziekte
zeldzame ziekte
arthrogryposis
GENETIC ASSOCIATION
UBA1

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