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Spinal muscular atrophy with congenital bone fractures 2

MONDO:0014807

Any prenatal-onset spinal muscular atrophy with congenital bone fractures in which the cause of the disease is a mutation in the ASCC1 gene.

Also known as: ASCC1 prenatal-onset spinal muscular atrophy with congenital bone fractures, SMABF2, prenatal-onset spinal muscular atrophy with congenital bone fractures caused by mutation in ASCC1, spinal muscular atrophy with congenital bone fractures 2, spinal muscular atrophy with congenital bone fractures type 2

11 clinical trials for this condition and its sub-types, 0 tagged with Spinal muscular atrophy with congenital bone fractures 2 itself.

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