inherited renal tubular disease pseudohypoaldosteronism type 1 https://github.com/monarch-initiative/mondo/issues/7273 https://github.com/monarch-initiative/mondo/issues/7766 https://www.malacards.org/card/pseudohypoaldosteronism_type_1 OMIMPS:177735 ICD9:275.8 A rare, primary form of mineralocorticoid resistance characterized by mild to profound salt wasting either restricted to the kidney (renal pseudohypoaldosteronism type 1), or generalized affecting many organs (generalized pseudohypoaldosteronism type 1). Clinical presentation is in the neonatal period with failure to thrive, vomiting and dehydration with biochemical findings of hyperkalaemia, metabolic acidosis and, elevated plasma aldosterone and renin concentration. icd11.foundation:1576878036 pseudohypoaldosteronism type I autosomal recessive Orphanet:756 PHA1B MONDO:0019161 GARD:0016545 MEDGEN:82805 UMLS:C0268436 NANDO:2200368 SCTID:43941006 NCIT:C123251 pseudohypoaldosteronism, type I PHA type 1 inherited pseudohypoaldosteronism