pseudohypoaldosteronism, type IB1, autosomal recessive (Monarch Disease Ontology identifier MONDO_0009917) can be described as follows. Generalized pseudohypoaldosteronism type 1 (generalized PHA1) is a severe form of primary mineralocorticoid resistance with systemic involvement and salt loss in multiple organs. Also known as: PHA1B, autosomal recessive PHA 1, autosomal recessive pseudohypoaldosteronism type 1, generalised PHA1, generalised pseudohypoaldosteronism type 1, generalized PHA1, generalized pseudohypoaldosteronism type 1.