pseudohyperaldosteronism type 2

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
pseudohyperaldosteronism type 2
NR3C2 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with pseudohyperaldosteronism type 2.
5 View disease cluster →
Pseudohypoaldosteronism 1 shared geneNR3C2 Related via 1 shared gene including NR3C2. Early-onset hypertension with severe exacerbation in pregnancy 1 shared geneNR3C2 Related via 1 shared gene including NR3C2. Pseudohypoparathyroidism 1 shared geneNR3C2 Related via 1 shared gene including NR3C2. Ventricular dysfunction 1 shared geneNR3C2 Related via 1 shared gene including NR3C2. Rolandic epilepsy 1 shared geneNR3C2 Related via 1 shared gene including NR3C2.