Prenatal spinal muscular atrophy and congenital bone fractures

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Subtype of: Spinal muscular atrophy
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • prenatal spinal muscular atrophy and congenital bone fractures
MONDO_0014806MONDO_0014807
ASCC1 Unknown
26924529 28218388 30327447 32160656 33931933 35838082 37455927 41230573
Open Targets
  • prenatal spinal muscular atrophy and congenital bone fractures
MONDO_0014806MONDO_0014807
TRIP4 Unknown
26924529 27008887 34075209 35276412 38143368
Open Targets —
All2 Causal0 Unknown2
Related Diseases Diseases that share the most curated genes with Prenatal spinal muscular atrophy and congenital bone fractures.
5 View disease cluster →
Spinal muscular atrophy with congenital bone fractures 2 1 shared geneASCC1 Related via 1 shared gene including ASCC1. Spinal muscular atrophy with congenital bone fractures 1 1 shared geneTRIP4 Related via 1 shared gene including TRIP4. Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome 1 shared geneTRIP4 Related via 1 shared gene including TRIP4. Hypotonia 1 shared geneASCC1 Related via 1 shared gene including ASCC1. Centronuclear myopathy 2 shared genesASCC1, TRIP4 Related via 2 shared genes including ASCC1, TRIP4.