Neurometabolic disorder

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
neurometabolic disorder
MONDO_0005066MONDO_0014072
FARS2 Unknown
27095821 27549011 28043061 29126765 29326872
Open Targets
SLC25A1 Unknown
23561848 27306203 29226520
Open Targets
neurometabolic disorder due to serine deficiency
PSAT1 Causal — ClinGen
PHGDH Unknown — ClinGen
PSPH Unknown — ClinGen
All5 Causal1 Unknown4
Related Diseases Diseases that share the most curated genes with Neurometabolic disorder.
5 View disease cluster →
Neu-laxova syndrome 3 shared genesPHGDH, PSPH, PSAT1 Related via 3 shared genes including PHGDH, PSPH, PSAT1. Phosphoglycerate dehydrogenase deficiency 1 shared genePHGDH Related via 1 shared gene including PHGDH. Neu-laxova syndrome 1 1 shared genePHGDH Related via 1 shared gene including PHGDH. Phosphoserine phosphatase deficiency 1 shared genePSPH Related via 1 shared gene including PSPH. Spastic paraplegia 77, autosomal recessive 1 shared geneFARS2 Related via 1 shared gene including FARS2.