Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
142365010 |
Pseudohypoaldosteronism, type 1, dominant form |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
142366011 |
Classic pseudohypoaldosteronism |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
828026014 |
Pseudohypoaldosteronism, type 1, dominant form (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
142365010 |
Pseudohypoaldosteronism, type 1, dominant form |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
142365010 |
Pseudohypoaldosteronism, type 1, dominant form |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
142366011 |
Classic pseudohypoaldosteronism |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
142366011 |
Classic pseudohypoaldosteronism |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
828026014 |
Pseudohypoaldosteronism, type 1, dominant form (disorder) |
en |
Fully specified name |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
828026014 |
Pseudohypoaldosteronism, type 1, dominant form (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
4670731000241117 |
pseudohypoaldostéronisme de type 1, dominant |
fr |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
4670731000241117 |
pseudohypoaldostéronisme de type 1, dominant |
fr |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships |
Type |
Target |
Active |
Characteristic |
Refinability |
Group |
Values |
Pseudohypoaldosteronism, type 1, dominant form |
Is a |
Reproductive system hereditary disorder (disorder) |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Pseudohypoaldosteronism, type 1, dominant form |
Is a |
Hereditary disorder of endocrine system (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Pseudohypoaldosteronism, type 1, dominant form |
Is a |
Autosomal dominant hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Pseudohypoaldosteronism, type 1, dominant form |
Is a |
Pseudohypoaldosteronism, type 1 |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Pseudohypoaldosteronism, type 1, dominant form |
Finding site |
Adrenal cortex structure |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Pseudohypoaldosteronism, type 1, dominant form |
Finding site |
Entire endocrine gonad (body structure) |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Pseudohypoaldosteronism, type 1, dominant form |
Occurrence |
Congenital |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Pseudohypoaldosteronism, type 1, dominant form |
Finding site |
Adrenal cortex structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|