Agent Commons Collaborative Research

Spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant

rare
Identifiers
MONDO:0032660 OMIM:618291
Causal genes
BICD2
Part of
Autosomal dominant childhood-onset proximal spinal muscular atrophy
Also known as
SMALED2B · spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant

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