Pseudohypoaldosteronism type i, autosomal dominant

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Subtype of: Pseudohypoaldosteronism
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Pseudohypoaldosteronism type I, autosomal dominant
MONDO_0008329
NR3C2 Unknown
16972228 12788847 16954160 12483305 9662404
Open Targets
All1 Causal0 Unknown1
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Early-onset hypertension with severe exacerbation in pregnancy 1 shared geneNR3C2 Related via 1 shared gene including NR3C2. Pseudohyperaldosteronism type 2 1 shared geneNR3C2 Related via 1 shared gene including NR3C2. Pseudohypoaldosteronism 1, autosomal dominant 1 shared geneNR3C2 Related via 1 shared gene including NR3C2. Pseudohypoaldosteronism 1 shared geneNR3C2 Related via 1 shared gene including NR3C2. Pseudohypoparathyroidism 1 shared geneNR3C2 Related via 1 shared gene including NR3C2.