Application Version: 4.0.6.10
Content Version: 2024.07.12
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Code System Concept
Code System Concept Code | 472315005 |
Code System Concept Name | Mitochondrial cardiomyopathy (disorder) |
Code System Preferred Concept Name | Mitochondrial cardiomyopathy (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Superseded By Concept | |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 | 01/31/2013 |
SDO Date Created | 01/31/2013 |
SDO Date Revised | 01/31/2013 |
Description | |
Sequence |
Extended Properties
No extended properties.
Concept Alternate Designations
SDO Designation ID | Concept Designation Description | Status | Designation Type | PHIN Preferred Term Flag | Code Flag |
---|---|---|---|---|---|
2951138016 | Mitochondrial cardiomyopathy | Active | Synonym | false | false |
Parent Concepts
Parent Concepts
|
Other Relationships
No other relationships present.
|
Child Concepts
Mitochondrial cardiomyopathy (disorder) {472315005 , SNOMED-CT }
Parent/Child (Relationship Type)
Combined oxidative phosphorylation defect type 23 (disorder)
{1173036000
, SNOMED-CT
}
Dilated cardiomyopathy due to mitochondrial disease (disorder)
{871639003
, SNOMED-CT
}
Fatal infantile mitochondrial cardiomyopathy (disorder)
{472319004
, SNOMED-CT
}
Histiocytoid mitochondrial cardiomyopathy (disorder)
{472317002
, SNOMED-CT
}
Hypertrophic mitochondrial cardiomyopathy (disorder)
{472316006
, SNOMED-CT
}
Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome (disorder)
{1172839002
, SNOMED-CT
}
Maternally inherited mitochondrial cardiomyopathy (disorder)
{1187635008
, SNOMED-CT
}
Maternally inherited mitochondrial cardiomyopathy and myopathy (disorder)
{472320005
, SNOMED-CT
}
|
- Page last reviewed:June 20, 2024
- Page last updated:June 20, 2024
- Content source: