Peripheral motor neuropathy, childhood-onset, biotin-responsive

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Peripheral motor neuropathy, childhood-onset, biotin-responsive
MONDO_0859255
SLC5A6 Causal
35013551 27904971
Open Targets
All1 Causal1 Unknown0
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Neurodegeneration, infantile-onset, biotin-responsive 1 shared geneSLC5A6 Related via 1 shared gene including SLC5A6. Sodium-dependent multivitamin transporter deficiency 1 shared geneSLC5A6 Related via 1 shared gene including SLC5A6. Genetic neurodegenerative disease 1 shared geneSLC5A6 Related via 1 shared gene including SLC5A6. Uterine fibroid 1 shared geneSLC5A6 Related via 1 shared gene including SLC5A6. Neurodevelopmental disorder 1 shared geneSLC5A6 Related via 1 shared gene including SLC5A6.