Phenotypes for disease #02214 (SMAX2 (atrophy, muscular, spinal, X-linked, type 2, infantile (SMAX-2, arthrogryposis multiplex congenita, distal, X-linked)), OMIM:301830)

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0000138573 - X-linked congenital spinal muscular atrophy SMAX-2 Familial, X-linked recessive - - - ? - Alfons Meindl 00173709
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