encephalopathy, progressive, with amyotrophy and optic atrophy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Encephalopathy, progressive, with amyotrophy and optic atrophy
TBCE Causal
27666369
ClinGen —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with encephalopathy, progressive, with amyotrophy and optic atrophy.
5 View disease cluster →
Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome 1 shared geneTBCE Related via 1 shared gene including TBCE. Sanjad-sakati syndrome 1 shared geneTBCE Related via 1 shared gene including TBCE. Kenny-caffey syndrome 1 shared geneTBCE Related via 1 shared gene including TBCE. Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome 1 shared geneTBCE Related via 1 shared gene including TBCE. Osteosclerosis 1 shared geneTBCE Related via 1 shared gene including TBCE.