Methylmalonic aciduria, cblb type

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Subtype of: Methylmalonic acidemia
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation type
EFO_0009074
MMAB Unknown
27604308
Open Targets
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Methylmalonic aciduria, cblb type.
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Hyper-immunoglobulin d syndrome 1 shared geneMMAB Related via 1 shared gene including MMAB. Polymyositis 1 shared geneMMAB Related via 1 shared gene including MMAB. Methylmalonic acidemia 1 shared geneMMAB Related via 1 shared gene including MMAB. Autoinflammatory syndrome 1 shared geneMMAB Related via 1 shared gene including MMAB. Cataract 1 shared geneMMAB Related via 1 shared gene including MMAB.