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SNOMED CT
Last uploaded:
August 28, 2024
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| Preferred Name | Aldosterone deficiency | |
| Synonyms |
Aldosterone deficiency (disorder) Hypoaldosteronism |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/60086000 |
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| Active |
1
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|
| altLabel |
Aldosterone deficiency (disorder) Hypoaldosteronism
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|
| CASE SIGNIFICANCE ID |
900000000000020002 900000000000448009
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|
| CTV3ID |
C1543
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|
| cui |
C0020595
|
|
| DEFINITION STATUS ID |
900000000000074008
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|
| Effective time |
20020131
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| Has finding site | ||
| notation |
60086000
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|
| prefLabel |
Aldosterone deficiency
|
|
| Subset member |
6011000124106~MAPADVICE~IF FAMILIAL ALDOSTERONE DEFICIENCY CHOOSE E27.49 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~E27.49 447562003~MAPTARGET~E27.4 447562003~MAPRULE~TRUE 6011000124106~MAPPRIORITY~7 6011000124106~MAPPRIORITY~4 6011000124106~MAPRULE~IFA 236464008 | Hyporeninemic hypoaldosteronism | 6011000124106~MAPRULE~IFA 715343000 | Familial aldosterone deficiency (disorder) | 6011000124106~MAPRULE~IFA 47757001 | Corticosterone 18-monooxygenase deficiency | 447562003~MAPADVICE~ALWAYS E27.4 6011000124106~MAPRULE~IFA 1186812001 | Familial hyperreninemic hypoaldosteronism type 2 | 6011000124106~MAPADVICE~IF CORTICOSTERONE 18-MONOOXYGENASE DEFICIENCY CHOOSE E25.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPGROUP~1 6011000124106~MAPRULE~IFA 1217069000 | Familial hyperreninemic hypoaldosteronism type 1B | 6011000124106~MAPPRIORITY~8 6011000124106~MAPRULE~IFA 715343000 | Familial hypoaldosteronism | 6011000124106~MAPADVICE~IF FAMILIAL HYPERRENINEMIC HYPOALDOSTERONISM TYPE 2 CHOOSE E27.49 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000508004~ACCEPTABILITYID~900000000000549004 6011000124106~MAPADVICE~IF FAMILIAL HYPOALDOSTERONISM CHOOSE E27.49 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 237765003 | Hyperreninemic hypoaldosteronism | 447562003~MAPGROUP~1 6011000124106~MAPTARGET~E25.0 447562003~CORRELATIONID~447561005 6011000124106~MAPCATEGORYID~447637006 900000000000509007~ACCEPTABILITYID~900000000000548007 6011000124106~MAPRULE~IFA 1217075009 | Familial hyperreninemic hypoaldosteronism type 1A | 900000000000508004~ACCEPTABILITYID~900000000000548007 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 6011000124106~MAPADVICE~IF HYPORENINEMIC HYPOALDOSTERONISM CHOOSE E27.49 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPTARGET~E27.40 6011000124106~MAPPRIORITY~5 6011000124106~MAPADVICE~IF FAMILIAL HYPERRENINEMIC HYPOALDOSTERONISM TYPE 1A CHOOSE E27.49 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPCATEGORYID~447639009 6011000124106~MAPRULE~IFA 236464008 | Hyporeninemic hypoaldosteronism (disorder) | 6011000124106~MAPADVICE~ALWAYS E27.40 6011000124106~MAPADVICE~IF HYPERRENINEMIC HYPOALDOSTERONISM CHOOSE E27.49 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~1 6011000124106~MAPPRIORITY~6 900000000000497000~MAPTARGET~C1543 6011000124106~CORRELATIONID~447561005 6011000124106~MAPRULE~IFA 47757001 | Corticosterone 18-monooxygenase deficiency (disorder) | 6011000124106~MAPPRIORITY~3 900000000000509007~ACCEPTABILITYID~900000000000549004 6011000124106~MAPPRIORITY~2 6011000124106~MAPRULE~IFA 237765003 | Hyperreninemic hypoaldosteronism (disorder) | 6011000124106~MAPADVICE~IF FAMILIAL HYPERRENINEMIC HYPOALDOSTERONISM TYPE 1B CHOOSE E27.49 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
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|
| tui |
T047
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|
| Type ID |
900000000000003001 900000000000013009
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| subClassOf |
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