Spastic paraplegia 79a, autosomal dominant

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Subtype of: Spastic paraplegia · Spastic paraplegia 79
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Spastic paraplegia 79A, autosomal dominant
MONDO_0859363
UCHL1 Unknown
23359680 29735986 33159930 32656641 11555633 35986737 28007905 10048490
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Spastic paraplegia 79a, autosomal dominant.
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Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome 1 shared geneUCHL1 Related via 1 shared gene including UCHL1. Spastic paraplegia 79b, autosomal recessive 1 shared geneUCHL1 Related via 1 shared gene including UCHL1. Parkinson disease 5, autosomal dominant, susceptibility to 1 shared geneUCHL1 Related via 1 shared gene including UCHL1. Peripheral nervous system disease 1 shared geneUCHL1 Related via 1 shared gene including UCHL1. Non-neoplastic peripheral nervous system disease 1 shared geneUCHL1 Related via 1 shared gene including UCHL1.