Encephalopathy, progressive, with amyotrophy and optic atrophy

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Subtype of: Encephalopathy
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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
MONDO_0014968
TBCE Causal
27666369
ClinGen, Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Encephalopathy, progressive, with amyotrophy and optic atrophy.
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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. Hypoparathyroidism-retardation-dysmorphism syndrome 1 shared geneTBCE Related via 1 shared gene including TBCE. Caffey syndrome, type 1 1 shared geneTBCE Related via 1 shared gene including TBCE. Kenny-caffey syndrome 1 shared geneTBCE Related via 1 shared gene including TBCE.