Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome

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Subtype of: Congenital muscular dystrophy
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome
MONDO_0014896
TRIP4 Causal
26924529 27008887
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome.
5 View disease cluster →
Spinal muscular atrophy with congenital bone fractures 1 1 shared geneTRIP4 Related via 1 shared gene including TRIP4. Prenatal spinal muscular atrophy and congenital bone fractures 1 shared geneTRIP4 Related via 1 shared gene including TRIP4. Pericarditis 1 shared geneTRIP4 Related via 1 shared gene including TRIP4. Centronuclear myopathy 1 shared geneTRIP4 Related via 1 shared gene including TRIP4. Congenital muscular dystrophy 1 shared geneTRIP4 Related via 1 shared gene including TRIP4.