Cerebral atrophy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CEREBRAL ATROPHY
C0235946
EXOSC9 Causal — Disgenet
All7 Causal1 Unknown6
Related Diseases Diseases that share the most curated genes with Cerebral atrophy.
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Intellectual developmental disorder expressive speech dysmorphic 1 shared geneSETBP1 Related via 1 shared gene including SETBP1. Schinzel-Giedion syndrome 1 shared geneSETBP1 Related via 1 shared gene including SETBP1. Cerebellar ataxia with deafness and narcolepsy 1 shared geneDNMT1 Related via 1 shared gene including DNMT1. Cerebellar ataxia, deafness, and narcolepsy 1 shared geneDNMT1 Related via 1 shared gene including DNMT1. hyperinsulinemic hypoglycemia with polycystic kidney disease 1 shared genePMM2 Related via 1 shared gene including PMM2.