Title : Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene.

Pub. Date : 2016

PMID : 26807262






2 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 UNLABELLED: Autosomal recessive pseudohypoaldosteronism type 1 (PHA1) is a rare disorder characterized by sodium wasting, failure to thrive, hyperkalemia, hypovolemia and metabolic acidosis. Sodium sodium channel epithelial 1 subunit gamma Homo sapiens
2 UNLABELLED: Autosomal recessive pseudohypoaldosteronism type 1 (PHA1) is a rare disorder characterized by sodium wasting, failure to thrive, hyperkalemia, hypovolemia and metabolic acidosis. Sodium sodium channel epithelial 1 subunit gamma Homo sapiens