Number of the records: 1
pseudohypoaldosteronizmus
Record number d011546 Date 06.06.2025 Type M - MESH Topical term pseudohypoaldosteronizmus Other term English (Pseudonym) Gordon Hyperkalemia-Hypertension Syndrome
English (Pseudonym) Hyperpotassemia and Hypertension, Familial
English (Pseudonym) Hypertensive Hyperkalemia, Familial
English (Pseudonym) Pseudohypoaldosteronism Type 1
English (Pseudonym) Pseudohypoaldosteronism Type 1, Autosomal Recessive
English (Pseudonym) Pseudohypoaldosteronism, Type I
English (Pseudonym) Pseudohypoaldosteronism, Type I, Autosomal Dominant
English (Pseudonym) Pseudohypoaldosteronism, Type I, Autosomal Recessive
English (Pseudonym) Pseudohypoaldosteronism, Type II
Slovak (Pseudonym) Gordonov syndróm hyperkaliémie a hypertenzie
Slovak (Pseudonym) hyperkaliémia a hypertenzia familiárna
Slovak (Pseudonym) hyperkaliémia hypertenzívna familiárna
Slovak (Pseudonym) pseudohypoaldosteronizmus, typ 1
Slovak (Pseudonym) pseudohypoaldosteronizmus, typ I
pseudohypoaldosteronizmus typu 1
Slovak (Pseudonym) pseudohypoaldosteronizmus typu 1, autozomálne recesívny
Slovak (Pseudonym) pseudohypoaldosteronizmus typu I, autozomálne dominantný
Slovak (Pseudonym) pseudohypoaldosteronizmus typu I, autozomálne recesívny
Slovak (Pseudonym) pseudohypoaldosteronizmus typu II
See also (Later heading) aldosterón
(Skutočné meno) receptory mineralokortikoidové
(Skutočné meno) kanály epitelové sodíkové
UDC C12.050.351.968.419.815.770C12.200.777.419.815.770C12.950.419.815.770C16.320.831.770 Note A heterogeneous group of disorders characterized by renal electrolyte transport dysfunctions. Congenital forms are rare autosomal disorders characterized by neonatal hypertension, HYPERKALEMIA, increased RENIN activity and ALDOSTERONE concentration. The Type I features HYPERKALEMIA with sodium wasting; Type II, HYPERKALEMIA without sodium wasting. Pseudohypoaldosteronism can be the result of a defective renal electrolyte transport protein or acquired after KIDNEY TRANSPLANTATION. 
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Number of the records: 1