Preferred Name |
Apparent mineralocorticoid excess |
|
Synonyms |
Ulick syndrome |
|
Definitions |
A rare form of pseudohyperaldosteronism characterized by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism. |
|
ID |
http://www.orpha.net/ORDO/Orphanet_320 |
|
alternative_term |
Ulick syndrome 11-beta-hydroxysteroid dehydrogenase deficiency type 2 |
|
definition |
A rare form of pseudohyperaldosteronism characterized by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism. |
|
definition_citation |
Orphanet |
|
expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=320 |
|
has_age_of_onset |
Infancy Neonatal |
|
has_inheritance |
Autosomal recessive |
|
hasDbXref |
MeSH:D043204 UMLS:C0342488 ICD-10:E26.8 ICD-11:5A76.Y OMIM:218030 MedDRA:10080229 |
|
label |
Apparent mineralocorticoid excess |
|
notation |
ORPHA:320 |
|
part_of |
http://www.orpha.net/ORDO/Orphanet_506213 http://www.orpha.net/ORDO/Orphanet_156629 |
|
prefixIRI |
ORDO:Orphanet_320 |
|
prefLabel |
Apparent mineralocorticoid excess |
|
present_in |
Europe AND has_point_prevalence_range : <1 / 1 000 000 |
|
treeView |
http://www.orpha.net/ORDO/Orphanet_506213 http://www.orpha.net/ORDO/Orphanet_156629 |
|
subClassOf |