Spinal muscular atrophy, lower extremity predominant, 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
Spinal muscular atrophy, lower extremity-predominant, AD
MONDO_0008026
DYNC1H1 Unknown
21820100 22368300 22459677 24307404 24896178 25484024 25529582 25609763 26392352 27066557 27331017 28193117 28554554 29306600 30122514
Open Targets
All1 Causal0 Unknown1
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Severe intellectual disability with neuronal migration disorder 1 shared geneDYNC1H1 Related via 1 shared gene including DYNC1H1. Neuronal migration abnormalities 1 shared geneDYNC1H1 Related via 1 shared gene including DYNC1H1. Spinal muscular atrophy, lower extremity-predominant 1, autosomal dominant 1 shared geneDYNC1H1 Related via 1 shared gene including DYNC1H1. Mental retardation, autosomal dominant 13 1 shared geneDYNC1H1 Related via 1 shared gene including DYNC1H1. Childhood-onset spinal muscular atrophy 1 shared geneDYNC1H1 Related via 1 shared gene including DYNC1H1.