infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development
GLS Causal
30239721
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development.
5 View disease cluster →
Casgid syndrome 1 shared geneGLS Related via 1 shared gene including GLS. Glutaminase deficiency 1 shared geneGLS Related via 1 shared gene including GLS. B-cell acute lymphoblastic leukemia 1 shared geneGLS Related via 1 shared gene including GLS. Myositis 1 shared geneGLS Related via 1 shared gene including GLS. Generalized epilepsy 1 shared geneGLS Related via 1 shared gene including GLS.