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.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Prenatal-onset spinal muscular atrophy with congenital bone fractures (0)

Including sub-types (11) Tagged with Spinal muscular atrophy with congenital bone fractures 2 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.