Application Version: 4.0.6.10
Content Version: 2024.07.12
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Code System Concept
Code System Concept Code | 720610008 |
Code System Concept Name | Cardiomyopathy and renal anomaly syndrome (disorder) |
Code System Preferred Concept Name | Cardiomyopathy and renal anomaly syndrome (disorder) |
Concept Status | Published |
Concept Status Date | 09/01/2024 |
Code System Name | SNOMED-CT |
Concept Details
Code System Code | PH_SNOMED-CT |
Code System OID | 2.16.840.1.113883.6.96 |
HL7 Table 0396 Code | SCT |
Superseded By Concept | |
SDO Concept Status | Active |
SDO Concept Status Date | 01/31/2017 |
SDO Date Created | 01/31/2017 |
SDO Date Revised | 01/31/2017 |
Description | 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. |
Sequence |
Extended Properties
No extended properties.
Concept Alternate Designations
SDO Designation ID | Concept Designation Description | Status | Designation Type | PHIN Preferred Term Flag | Code Flag |
---|---|---|---|---|---|
3321533010 | Cardiomyopathy and renal anomaly syndrome | Active | Synonym | false | false |
Parent Concepts
Parent Concepts
Parent/Child (Relationship Type)
Cardiovascular system hereditary disorder (disorder)
{363005004
, SNOMED-CT
}
Congenital anomaly of myocardium (disorder)
{204394002
, SNOMED-CT
}
Congenital cardiovascular disorder (disorder)
{762228008
, SNOMED-CT
}
Developmental hereditary disorder (disorder)
{363070008
, SNOMED-CT
}
Genitourinary congenital anomalies (disorder)
{287085006
, SNOMED-CT
}
Hypertrophic cardiomyopathy (disorder)
{233873004
, SNOMED-CT
}
|
Other Relationships
No other relationships present.
|
Child Concepts
No child concepts present.
|
- Page last reviewed:June 20, 2024
- Page last updated:June 20, 2024
- Content source: