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SNOMED CT, US Edition
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/SNOMEDCT/720610008
http://purl.bioontology.org/ontology/SNOMEDCT/720610008
|
|---|---|
| Preferred Name | Cardiomyopathy and renal anomaly syndrome |
| Definitions |
The association of hypertrophic cardiomyopathy with variable malformations of the urogenital tract. To date, it has been described in two brothers born to nonconsanguineous parents. One of the brothers also had dysgenesis of the corpus callosum. The mode of transmission is unknown but may be X-linked or autosomal recessive.
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| Synonyms |
Cardiomyopathy and renal anomaly syndrome (disorder)
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | The association of hypertrophic cardiomyopathy with variable malformations of the urogenital tract. To date, it has been described in two brothers born to nonconsanguineous parents. One of the brothers also had dysgenesis of the corpus callosum. The mode of transmission is unknown but may be X-linked or autosomal recessive. |
|---|---|
| altLabel | Cardiomyopathy and renal anomaly syndrome (disorder)
|
| prefLabel | Cardiomyopathy and renal anomaly syndrome
|
| Type ID |
900000000000003001
900000000000013009
|
| CASE SIGNIFICANCE ID | 900000000000448009
|
| notation | 720610008
|
| Effective time | 20170131
|
| Active | 1
|
| Has finding site | |
| Has pathological process | |
| subClassOf | |
| Semantic type UMLS property | |
| type | |
| Subset member | 447562003~MAPRULE~TRUE
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
6011000124106~MAPADVICE~ALWAYS Q63.9
447562003~MAPTARGET~Q87.8
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
900000000000508004~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~ALWAYS I42.4 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
6011000124106~MAPTARGET~Q63.9
447562003~MAPADVICE~ALWAYS Q87.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
6011000124106~MAPRULE~TRUE
6011000124106~MAPTARGET~I42.4
900000000000497000~MAPTARGET~XUuCj
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| DEFINITION STATUS ID | 900000000000074008
|
| tui | T047
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| CTV3ID | XUuCj
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| Occurs in | |
| cui | C4303967
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| Has associated morphology |
| Delete | Subject | Author | Type | Created |
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| No notes to display |