Congenital muscular hypertrophy-cerebral syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL MUSCULAR HYPERTROPHY-CEREBRAL SYNDROME
C1802395
SMC1A Causal — ClinVar, Disgenet
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Congenital muscular hypertrophy-cerebral syndrome.
5 View disease cluster →
Wiedemann-steiner syndrome 1 shared geneSMC1A Related via 1 shared gene including SMC1A. De lange syndrome 1 shared geneSMC1A Related via 1 shared gene including SMC1A. Cornelia de lange syndrome 1 shared geneSMC1A Related via 1 shared gene including SMC1A. Congenital pes cavus 1 shared geneSMC1A Related via 1 shared gene including SMC1A. Rett syndrome 1 shared geneSMC1A Related via 1 shared gene including SMC1A.