Autosomal dominant, spinal muscular atrophy, lower extremity-predominant, 2b, autosomal dominant

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Subtype of: Spinal muscular atrophy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
autosomal dominant, Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant
EFO_0010264
BICD2 Unknown
27751653 28635954 29274205 30054298
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Autosomal dominant, spinal muscular atrophy, lower extremity-predominant, 2b, autosomal dominant.
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Reduced fetal movements 1 shared geneBICD2 Related via 1 shared gene including BICD2. Pterygium 1 shared geneBICD2 Related via 1 shared gene including BICD2. Spinal muscular atrophy, lower extremity-predominant, 2, autosomal dominant 1 shared geneBICD2 Related via 1 shared gene including BICD2. Spinal muscular atrophy, lower extremity-predominant 2a, childhood onset, autosomal dominant 1 shared geneBICD2 Related via 1 shared gene including BICD2. Spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant 1 shared geneBICD2 Related via 1 shared gene including BICD2.