Monocarboxylate transporter 1 deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Monocarboxylate transporter 1 deficiency
MONDO_0014490
SLC16A1 Unknown
26608392 17701893 25390740 33333023
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Monocarboxylate transporter 1 deficiency.
5 View disease cluster →
Fatty acid and ketone body metabolism disorder 1 shared geneSLC16A1 Related via 1 shared gene including SLC16A1. Fatty acid oxidation and ketone body metabolism disorder 1 shared geneSLC16A1 Related via 1 shared gene including SLC16A1. Erythrocyte lactate transporter defect 1 shared geneSLC16A1 Related via 1 shared gene including SLC16A1. Symptomatic deficiency in lactate transport 1 shared geneSLC16A1 Related via 1 shared gene including SLC16A1. Hyperinsulinemic hypoglycemia 1 shared geneSLC16A1 Related via 1 shared gene including SLC16A1.