Congenital nad deficiency disorder

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
congenital NAD deficiency disorder
MONDO_0020831
NADSYN1 Causal
31883644 35491967
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Congenital nad deficiency disorder.
5 View disease cluster →
Congenital vertebral-cardiac-renal anomalies syndrome 1 shared geneNADSYN1 Related via 1 shared gene including NADSYN1. Smith-lemli-opitz syndrome 1 shared geneNADSYN1 Related via 1 shared gene including NADSYN1. Vertebral, cardiac, renal, and limb defects syndrome 1 shared geneNADSYN1 Related via 1 shared gene including NADSYN1. Vitamin deficiency disorder 1 shared geneNADSYN1 Related via 1 shared gene including NADSYN1. Hyperopia 1 shared geneNADSYN1 Related via 1 shared gene including NADSYN1.