pseudohypoaldosteronism type 2
Pseudohypoaldosteronism type 2 (PHA2) is a rare inherited form of hypertension characterized by hyperkalemia, hyperchloremic metabolic acidosis, normal or elevated aldosterone, low renin, and normal renal function
Press Enter · cited answer in seconds
0 sources
pseudohypoaldosteronism type 2
Summary
pseudohypoaldosteronism type 2 is a class of disease[1].
Key Facts
- pseudohypoaldosteronism type 2's instance of is recorded as class of disease[2].
- pseudohypoaldosteronism type 2's subclass of is recorded as pseudohypoaldosteronism[3].
- pseudohypoaldosteronism type 2's Orphanet ID is recorded as 757[4].
- pseudohypoaldosteronism type 2's NCI Thesaurus ID is recorded as C123252[5].
- pseudohypoaldosteronism type 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_757[6].
- pseudohypoaldosteronism type 2's UMLS CUI is recorded as C1449844[7].
- pseudohypoaldosteronism type 2's ICD-10-CM is recorded as I15.1[8].
- pseudohypoaldosteronism type 2's GARD rare disease ID is recorded as 4553[9].
- pseudohypoaldosteronism type 2's Mondo ID is recorded as MONDO_0019162[10].
- pseudohypoaldosteronism type 2's Genetics Home Reference Conditions ID is recorded as pseudohypoaldosteronism-type-2[11].