Spastic paraplegia 56, autosomal recessive, with or without pseudoxanthoma elasticum

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Subtype of: Spastic paraplegia · Spastic paraplegia 56, autosomal recessive
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Spastic paraplegia 56, autosomal recessive, with or without pseudoxanthoma elasticum
MONDO_0014015
CYP2U1 Unknown
23176821
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Spastic paraplegia 56, autosomal recessive, with or without pseudoxanthoma elasticum.
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Spastic paraplegia 56, autosomal recessive 1 shared geneCYP2U1 Related via 1 shared gene including CYP2U1. Retinal disorder 1 shared geneCYP2U1 Related via 1 shared gene including CYP2U1. Hereditary spastic paraplegia 1 shared geneCYP2U1 Related via 1 shared gene including CYP2U1. Congenital neurologic anomalies 1 shared geneCYP2U1 Related via 1 shared gene including CYP2U1. Spastic paraplegia 1 shared geneCYP2U1 Related via 1 shared gene including CYP2U1.