SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Prothrombin complex deficiency

Synonyms

Prothrombin complex deficiency (disorder)

ID

http://purl.bioontology.org/ontology/SNOMEDCT/234454002

Active

1

altLabel

Prothrombin complex deficiency (disorder)

CASE SIGNIFICANCE ID

900000000000448009

CTV3ID

X20EU

cui

C0398615

DEFINITION STATUS ID

900000000000074008

Effective time

20020131

Has interpretation

http://purl.bioontology.org/ontology/SNOMEDCT/263654008

interprets

http://purl.bioontology.org/ontology/SNOMEDCT/74848003

notation

234454002

prefLabel

Prothrombin complex deficiency

Subset member

6011000124106~MAPADVICE~IF ACQUIRED FACTOR II DEFICIENCY CHOOSE D68.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 2036003 | Acquired factor VII deficiency disease |

6011000124106~MAPRULE~IFA 191298004 | Acquired factor II deficiency (disorder) |

447562003~MAPRULE~TRUE

6011000124106~MAPADVICE~IF FACTOR X DEFICIENCY DUE TO SYSTEMIC AMYLOIDOSIS CHOOSE E85.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~4

6011000124106~MAPTARGET~D68.2

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

6011000124106~MAPADVICE~IF ACQUIRED FACTOR X DEFICIENCY DISEASE CHOOSE D68.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~

6011000124106~MAPCATEGORYID~447638001

6011000124106~MAPGROUP~1

6011000124106~MAPRULE~IFA 33820001 | Acquired factor X deficiency disease |

6011000124106~MAPGROUP~2

6011000124106~MAPTARGET~E85.9

447562003~MAPADVICE~ALWAYS D68.2 | MAPPED FOLLOWING WHO GUIDANCE

6011000124106~MAPRULE~IFA 33820001 | Acquired factor X deficiency disease (disorder) |

447562003~MAPGROUP~1

447562003~CORRELATIONID~447561005

6011000124106~MAPADVICE~IF FACTOR X DEFICIENCY DUE TO SYSTEMIC AMYLOIDOSIS CHOOSE D68.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

447562003~MAPTARGET~D68.2

900000000000508004~ACCEPTABILITYID~900000000000548007

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPPRIORITY~5

6011000124106~MAPADVICE~ALWAYS D68.2

6011000124106~MAPADVICE~IF ACQUIRED FACTOR VII DEFICIENCY DISEASE CHOOSE D68.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPRULE~IFA 191298004 | Acquired factor II deficiency |

6011000124106~MAPRULE~IFA 2036003 | Acquired factor VII deficiency disease (disorder) |

6011000124106~MAPPRIORITY~1

6011000124106~CORRELATIONID~447561005

6011000124106~MAPRULE~TRUE

900000000000497000~MAPTARGET~X20EU

6011000124106~MAPPRIORITY~3

6011000124106~MAPPRIORITY~2

6011000124106~MAPTARGET~D68.4

6011000124106~MAPRULE~IFA 1148862002 | Factor X deficiency due to systemic amyloidosis |

tui

T047

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/64779008

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