has material basis in germline mutation in SCNN1A pseudohypoaldosteronism, type IB1, autosomal recessive https://rarediseases.info.nih.gov/diseases/4552/autosomal-recessive-pseudohypoaldosteronism-type-1 https://www.malacards.org/card/pseudohypoaldosteronism_type_ib1_autosomal_recessive pseudohypoaldosteronism type 1, recessive generalized pseudohypoaldosteronism type 1 autosomal recessive PHA 1 OMIM:264350 GARD:0004552 MEDGEN:1823950 generalised PHA1 autosomal recessive pseudohypoaldosteronism type 1 pseudohypoaldosteronism type 1 autosomal recessive Generalized pseudohypoaldosteronism type 1 (generalized PHA1) is a severe form of primary mineralocorticoid resistance with systemic involvement and salt loss in multiple organs. MONDO:0009917 PHA1B PHA I, autosomal recessive UMLS:C5774176 generalised pseudohypoaldosteronism type 1 generalized PHA1 pseudohypoaldosteronism, type I, autosomal recessive Orphanet:171876 pseudohypoaldosteronism type 1