severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome
BCAP31 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome.
4 View disease cluster →
Contiguous abcd1-dxs1375e deletion syndrome 1 shared geneBCAP31 Related via 1 shared gene including BCAP31. Deafness, dystonia, and cerebral hypomyelination 1 shared geneBCAP31 Related via 1 shared gene including BCAP31. Global developmental delay 1 shared geneBCAP31 Related via 1 shared gene including BCAP31. Hearing loss 1 shared geneBCAP31 Related via 1 shared gene including BCAP31.