| Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
| 3008085015 |
Apparent mineralocorticoid excess |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
| 3008100012 |
Apparent mineralocorticoid excess (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
| 3008140018 |
AME - apparent mineralocorticoid excess |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
| 6186211000146117 |
11βHSD type 2-deficiëntie |
nl |
Synonym (core metadata concept) |
Inactive |
Only initial character case insensitive (core metadata concept) |
SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6186221000146110 |
deficiëntie van 11-bèta-hydroxysteroïddehydrogenase type 2 |
nl |
Synonym (core metadata concept) |
Inactive |
Entire term case insensitive (core metadata concept) |
SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6186241000146116 |
AME-syndroom |
nl |
Synonym (core metadata concept) |
Inactive |
Entire term case sensitive (core metadata concept) |
SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6186251000146118 |
'apparent mineralocorticoid excess'-syndroom |
nl |
Synonym (core metadata concept) |
Inactive |
Entire term case insensitive (core metadata concept) |
SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6641531000146110 |
syndroom van schijnbare mineralocorticoïdovermaat |
nl |
Synonym (core metadata concept) |
Inactive |
Entire term case insensitive (core metadata concept) |
SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6641541000146119 |
syndroom van schijnbare mineralocorticoïdovermaat (aandoening) |
nl |
Fully specified name |
Inactive |
Entire term case insensitive (core metadata concept) |
SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3008220019 |
A rare autosomal recessive disorder characterized by very early-onset and severe hypertension, low renin levels, low aldosterone, metabolic alkalosis, hypernatremia, and hypokalemia. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
| 3008223017 |
A rare autosomal recessive disorder characterised by very early-onset and severe hypertension, low renin levels, low aldosterone, metabolic alkalosis, hypernatraemia, and hypokalaemia. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
FHIR