Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome

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Subtype of: Congenital muscular dystrophy · Muscular dystrophy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome
MONDO_0859189
GGPS1 Causal
32403198 35869884
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome.
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Tubular aggregate myopathy 1 shared geneGGPS1 Related via 1 shared gene including GGPS1. Xx gonadal dysgenesis syndrome 1 shared geneGGPS1 Related via 1 shared gene including GGPS1. Perrault syndrome 1 shared geneGGPS1 Related via 1 shared gene including GGPS1. Neuromuscular disease 1 shared geneGGPS1 Related via 1 shared gene including GGPS1. Myopathy 1 shared geneGGPS1 Related via 1 shared gene including GGPS1.