Fibrinolytic bleeding syndrome

Fibrinolytic bleeding syndrome (disorder)

http://purl.bioontology.org/ontology/SNOMEDCT/234464006

1

Fibrinolytic bleeding syndrome (disorder)

900000000000448009

X20Ef

C0398619

900000000000074008

20020131

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

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

234464006

Fibrinolytic bleeding syndrome

6011000124106~MAPADVICE~ALWAYS D65 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE

6011000124106~MAPADVICE~IF HEREDITARY HYPOPLASMINOGENEMIA CHOOSE D68.8 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF HYPOPLASMINOGENEMIA CHOOSE E88.02 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~P53

447562003~MAPRULE~TRUE

6011000124106~MAPADVICE~IF CONGENITAL ALPHA-2-ANTIPLASMIN DEFICIENCY AND IF AGE AT ONSET OF CLINICAL FINDING BEFORE 29.0 DAYS CHOOSE P53 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 95842004 | Autosomal dominant deficiency of plasminogen |

6011000124106~MAPPRIORITY~7

6011000124106~MAPPRIORITY~4

6011000124106~MAPRULE~IFA 716746003 | Congenital alpha-2-antiplasmin deficiency |

6011000124106~MAPTARGET~D68.2

6011000124106~MAPGROUP~1

6011000124106~MAPADVICE~IF HYPOPLASMINOGENEMIA CHOOSE D68.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPADVICE~ALWAYS D65

6011000124106~MAPADVICE~IF ALPHA-2-ANTIPLASMIN DEFICIENCY CHOOSE D68.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 95842004 | Autosomal dominant deficiency of plasminogen (disorder) |

6011000124106~MAPPRIORITY~8

6011000124106~MAPTARGET~E88.02

6011000124106~MAPTARGET~D68.8

447562003~MAPGROUP~1

6011000124106~MAPRULE~IFA 234465007 | Alpha-2-antiplasmin deficiency (disorder) |

447562003~CORRELATIONID~447561005

6011000124106~MAPRULE~IFA 95840007 | Hypoplasminogenemia |

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~IF AUTOSOMAL DOMINANT DEFICIENCY OF PLASMINOGEN CHOOSE D68.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 95841006 | Hereditary hypoplasminogenemia |

6011000124106~MAPRULE~IFA 716746003 | Congenital alpha-2-antiplasmin deficiency (disorder) | AND IFA 445518008 | Age at onset of clinical finding (observable entity) | < 29.0 days

900000000000497000~MAPTARGET~X20Ef

6011000124106~MAPRULE~IFA 716746003 | Congenital alpha-2-antiplasmin deficiency | AND IFA 445518008 | Age at onset of clinical finding (observable entity) | < 29.0 days

6011000124106~MAPADVICE~IF ACQUIRED HYPOPLASMINOGENEMIA CHOOSE D68.8 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000508004~ACCEPTABILITYID~900000000000548007

447562003~MAPTARGET~D65

6011000124106~MAPRULE~IFA 95840007 | Hypoplasminogenemia (disorder) |

6011000124106~MAPRULE~IFA 234465007 | Alpha-2-antiplasmin deficiency |

6011000124106~MAPADVICE~IF CONGENITAL ALPHA-2-ANTIPLASMIN DEFICIENCY CHOOSE D68.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPPRIORITY~5

6011000124106~MAPRULE~IFA 95843009 | Acquired hypoplasminogenemia |

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPADVICE~IF CONGENITAL ALPHA-2-ANTIPLASMIN DEFICIENCY CHOOSE D68.8 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~D65

6011000124106~MAPPRIORITY~1

6011000124106~MAPPRIORITY~6

6011000124106~CORRELATIONID~447561005

6011000124106~MAPADVICE~IF ALPHA-2-ANTIPLASMIN DEFICIENCY CHOOSE D68.8 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~3

6011000124106~MAPRULE~IFA 716746003 | Congenital alpha-2-antiplasmin deficiency (disorder) |

6011000124106~MAPPRIORITY~2

T047

900000000000003001

900000000000013009

http://purl.bioontology.org/ontology/SNOMEDCT/95839005