HYPERALDOSTERONISM, FAMILIAL, TYPE II; HALD2

Question 1

What is  HYPERALDOSTERONISM, FAMILIAL, TYPE II; HALD2?

Accepted Answer

rare
autosomal dominant
not suppressible by dexamethasone

Question 2

Gibt es eine deutsche Bezeichnung?

Accepted Answer

Hyperaldosteronismus, familiärer, Typ II; Nebennierenrindenadenom , familiäres

Question 3

What is the link to OMIM ?

Accepted Answer

OMIN 605635

Disease	HYPERALDOSTERONISM, FAMILIAL, TYPE II; HALD2
OMIM	605635 OMIM = Online Mendelian Inheritance of Men
Orphanet	404
Gene locus	7p22
ICD	E26.0
Summary	rare autosomal dominant not suppressible by dexamethasone
Laboratory findings	Aldosterone inc (plasma)
Symptoms	adrenal hyperplasia hyperaldosteronism hypertension