Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect
MONDO:0060486Also known as: arthrogryposis multiplex congenita, neurogenic, with myelin defect, AMCNMY
1 clinical trial for this condition and its sub-types, 0 tagged with Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect itself.
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Including sub-types (1)
Tagged with Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect (0)