Spastic paraplegia 9b, autosomal recessive

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Subtype of: Spastic paraplegia
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Spastic paraplegia 9B, autosomal recessive
MONDO_0014702
ALDH18A1 Unknown
26297558 26026163 26320891 11092761 27604308 22170564 24816252 29903433
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Spastic paraplegia 9b, autosomal recessive.
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De barsy syndrome 1 shared geneALDH18A1 Related via 1 shared gene including ALDH18A1. P5CS deficiency 1 shared geneALDH18A1 Related via 1 shared gene including ALDH18A1. Developmental disorder-joint hypermobility-skin laxity with or without metabolic abnormalities 1 shared geneALDH18A1 Related via 1 shared gene including ALDH18A1. Cutis laxa, corneal clouding, and mental retardation 1 shared geneALDH18A1 Related via 1 shared gene including ALDH18A1. Cutis laxa, autosomal recessive, 3a 1 shared geneALDH18A1 Related via 1 shared gene including ALDH18A1.