Spinal muscular atrophy, lower extremity-predominant, 2, autosomal dominant

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Subtype of: Spinal muscular atrophy · Spinal muscular atrophy, lower extremity predominant, autosomal dominant
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Spinal muscular atrophy, lower extremity-predominant, 2, AD
MONDO_0014121
BICD2 Causal
25497877 23664116 24482476 30536747 23664120
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Spinal muscular atrophy, lower extremity-predominant, 2, 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. Autosomal dominant, spinal muscular atrophy, lower extremity-predominant, 2b, 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.