pseudohypoaldosteronism, type IB1, autosomal recessive

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
pseudohypoaldosteronism, type IB1, autosomal recessive
SCNN1A Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with pseudohypoaldosteronism, type IB1, autosomal recessive.
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Liddle syndrome 1 shared geneSCNN1A Related via 1 shared gene including SCNN1A. Pseudohypoparathyroidism 1 shared geneSCNN1A Related via 1 shared gene including SCNN1A. Bronchiectasis 1 shared geneSCNN1A Related via 1 shared gene including SCNN1A. Autoinflammatory syndrome 1 shared geneSCNN1A Related via 1 shared gene including SCNN1A. Proteinuria 1 shared geneSCNN1A Related via 1 shared gene including SCNN1A.