Methylmalonic aciduria and homocystinuria, cblx type

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Subtype of: Methylmalonic acidemia · Methylmalonic aciduria and homocystinuria
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Methylmalonic aciduria and homocystinuria, cblX type
MONDO_0010657
HCFC1 Unknown
23000143
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Methylmalonic aciduria and homocystinuria, cblx type.
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Mental retardation, x-linked 3 (methylmalonic acidemia and homocysteinemia, cblx type) 1 shared geneHCFC1 Related via 1 shared gene including HCFC1. Cobalamin c disease 1 shared geneHCFC1 Related via 1 shared gene including HCFC1. Intracellular cobalamin metabolism disorder 1 shared geneHCFC1 Related via 1 shared gene including HCFC1. Kabuki syndrome 1 shared geneHCFC1 Related via 1 shared gene including HCFC1. Methylmalonic acidemia 1 shared geneHCFC1 Related via 1 shared gene including HCFC1.