Methylmalonic aciduria and homocystinuria, cbld 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, cblD type
MONDO_0010185
MMADHC Unknown
18385497 19058814 27604308 24722857 26483544
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Methylmalonic aciduria and homocystinuria, cbld type.
5 View disease cluster →
Cobalamin metabolism disorder 1 shared geneMMADHC Related via 1 shared gene including MMADHC. Inborn disorder of cobalamin metabolism and transport 1 shared geneMMADHC Related via 1 shared gene including MMADHC. Methylmalonic aciduria, cbld type, variant 2 1 shared geneMMADHC Related via 1 shared gene including MMADHC. Homocystinuria, cbld type, variant 1 1 shared geneMMADHC Related via 1 shared gene including MMADHC. Homocystinuria with megaloblastic anemia 1 shared geneMMADHC Related via 1 shared gene including MMADHC.