Homocystinuria, cbld type, variant 1

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Subtype of: Homocystinuria
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Homocystinuria, cblD type, variant 1
MONDO_0010185
MMADHC Unknown
27604308
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Homocystinuria, cbld type, variant 1.
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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 and homocystinuria, cbld type 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 with megaloblastic anemia 1 shared geneMMADHC Related via 1 shared gene including MMADHC.