SNOMED CT

Last uploaded: August 28, 2024
Preferred Name

Familial cardiomyopathy
Synonyms

Familial cardiomyopathy (disorder)

Primary familial cardiomyopathy

ID

http://purl.bioontology.org/ontology/SNOMEDCT/35728003

Active

1

altLabel

Familial cardiomyopathy (disorder)

Primary familial cardiomyopathy

CASE SIGNIFICANCE ID

900000000000448009

CTV3ID

G5542

cui

C0264789

DEFINITION STATUS ID

900000000000073002

Effective time

20020131

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/74281007

notation

35728003

prefLabel

Familial cardiomyopathy

Subset member

6011000124106~MAPRULE~IFA 30884007 | Restrictive cardiomyopathy secondary to familial storage disease (disorder) |

6011000124106~MAPRULE~IFA 83978005 | Primary familial hypertrophic cardiomyopathy (disorder) |

6011000124106~MAPADVICE~ALWAYS I42.9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE

447562003~MAPRULE~TRUE

6011000124106~MAPADVICE~IF RESTRICTIVE CARDIOMYOPATHY SECONDARY TO FAMILIAL STORAGE DISEASE CHOOSE I43 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 766883006 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation |

6011000124106~MAPPRIORITY~7

6011000124106~MAPPRIORITY~4

6011000124106~MAPRULE~IFA 52029003 | Primary familial dilated cardiomyopathy |

6011000124106~MAPADVICE~IF DANISH TYPE FAMILIAL AMYLOID CARDIOMYOPATHY CHOOSE E85.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA

447562003~MAPTARGET~I42.5

6011000124106~MAPRULE~IFA 27097002 | Danish type familial amyloid cardiomyopathy |

6011000124106~MAPADVICE~IF FAMILIAL RESTRICTIVE CARDIOMYOPATHY CHOOSE I42.5 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~

6011000124106~MAPCATEGORYID~447638001

6011000124106~MAPADVICE~IF DILATED CARDIOMYOPATHY SECONDARY TO FAMILIAL STORAGE DISEASE CHOOSE E88.89 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPGROUP~1

6011000124106~MAPGROUP~2

6011000124106~MAPRULE~IFA 233878008 | Familial restrictive cardiomyopathy (disorder) |

6011000124106~MAPTARGET~E85.82

6011000124106~MAPADVICE~IF PRIMARY FAMILIAL HYPERTROPHIC CARDIOMYOPATHY CHOOSE I42.2 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~8

6011000124106~MAPADVICE~IF FAMILIAL DILATED CARDIOMYOPATHY WITH CONDUCTION DEFECT DUE TO LMNA MUTATION CHOOSE Q99.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000508004~ACCEPTABILITYID~900000000000549004

6011000124106~MAPRULE~IFA 83978005 | Primary familial hypertrophic cardiomyopathy |

6011000124106~MAPRULE~IFA 60514000 | Dilated cardiomyopathy secondary to familial storage disease |

6011000124106~MAPTARGET~I45.89

447562003~MAPGROUP~1

6011000124106~MAPRULE~IFA 715655000 | Transthyretin related familial amyloid cardiomyopathy |

447562003~CORRELATIONID~447561005

6011000124106~MAPRULE~IFA 52029003 | Primary familial dilated cardiomyopathy (disorder) |

6011000124106~MAPCATEGORYID~447637006

6011000124106~MAPTARGET~I42.2

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPRULE~IFA 471890009 | Dilated cardiomyopathy with genetic marker |

6011000124106~MAPRULE~IFA 27097002 | Danish type familial amyloid cardiomyopathy (disorder) |

900000000000508004~ACCEPTABILITYID~900000000000548007

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

6011000124106~MAPRULE~IFA 60514000 | Dilated cardiomyopathy secondary to familial storage disease (disorder) |

6011000124106~MAPADVICE~IF TRANSTHYRETIN RELATED FAMILIAL AMYLOID CARDIOMYOPATHY CHOOSE E85.82 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF PRIMARY FAMILIAL DILATED CARDIOMYOPATHY CHOOSE I42.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPPRIORITY~5

6011000124106~MAPRULE~IFA 715655000 | Transthyretin related familial amyloid cardiomyopathy (disorder) |

900000000000497000~MAPTARGET~G5542

6011000124106~MAPADVICE~IF DILATED CARDIOMYOPATHY SECONDARY TO FAMILIAL STORAGE DISEASE CHOOSE I42.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~9

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPADVICE~IF DILATED CARDIOMYOPATHY WITH GENETIC MARKER CHOOSE I42.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF RESTRICTIVE CARDIOMYOPATHY SECONDARY TO FAMILIAL STORAGE DISEASE CHOOSE E88.9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~I43

6011000124106~MAPADVICE~IF FAMILIAL DILATED CARDIOMYOPATHY WITH CONDUCTION DEFECT DUE TO LMNA MUTATION CHOOSE I45.89 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~I42.0

6011000124106~MAPTARGET~I42.9

6011000124106~MAPADVICE~IF TRANSTHYRETIN RELATED FAMILIAL AMYLOID CARDIOMYOPATHY CHOOSE I43 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~E88.9

6011000124106~MAPPRIORITY~1

6011000124106~MAPPRIORITY~6

6011000124106~MAPADVICE~IF FAMILIAL DILATED CARDIOMYOPATHY WITH CONDUCTION DEFECT DUE TO LMNA MUTATION CHOOSE I42.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~CORRELATIONID~447561005

447562003~MAPADVICE~ALWAYS I42.5

6011000124106~MAPTARGET~E88.89

6011000124106~MAPRULE~IFA 233878008 | Familial restrictive cardiomyopathy |

6011000124106~MAPGROUP~3

6011000124106~MAPTARGET~E85.4

6011000124106~MAPTARGET~I42.5

6011000124106~MAPRULE~IFA 30884007 | Restrictive cardiomyopathy secondary to familial storage disease |

6011000124106~MAPPRIORITY~3

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPPRIORITY~2

6011000124106~MAPTARGET~Q99.8

tui

T047

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/111941005

http://purl.bioontology.org/ontology/SNOMEDCT/85898001

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