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Searched for "Pseudohypoaldosteronism".

10 results found on Genetics Home Reference.

  • pseudohypoaldosteronism type 2 condition summary
    Found: Pseudohypoaldosteronism type 2 (PHA2) is a condition characterized...
    Related genes:
  • pseudohypoaldosteronism type 1 condition summary
    Found: Pseudohypoaldosteronism type 1 (PHA1) is a condition characterized...
    Related genes:
  • WNK4 gene summary
    Official name: WNK lysine deficient protein kinase 4
    Found: ...in the WNK4 gene can cause pseudohypoaldosteronism type 2 (PHA2), a condition characterized...
  • WNK1 gene summary
    Official name: WNK lysine deficient protein kinase 1
    Found: ...in the WNK1 gene can cause pseudohypoaldosteronism type 2 (PHA2), a condition characterized...
  • NR3C2 gene summary
    Official name: nuclear receptor subfamily 3, group C, member 2
    Found: ...been identified in people with pseudohypoaldosteronism type 1 (PHA1), a condition that...
  • SCNN1G gene summary
    Official name: sodium channel, non-voltage-gated 1, gamma subunit
    Found: ...involved in a condition called pseudohypoaldosteronism type 1 (PHA1). This condition typically...
  • SCNN1B gene summary
    Official name: sodium channel, non-voltage-gated 1, beta subunit
    Found: ...been identified in people with pseudohypoaldosteronism type 1 (PHA1). This condition typically...
  • SCNN1A gene summary
    Official name: sodium channel, non-voltage-gated 1 alpha subunit
    Found: ...in the SCNN1A gene cause pseudohypoaldosteronism type 1 (PHA1). This condition typically...
  • CUL3 gene information
    Official name: cullin 3
    Found: Pseudohypoaldosteronism 2E (PHA2E): An autosomal dominant...
  • KLHL3 gene information
    Official name: kelch-like family member 3
    Found: Pseudohypoaldosteronism 2D (PHA2D): A disorder characterized...
 
Published: November 24, 2014