1

Congenital omphalocele (disorder)

Amniocele

Omphalocele

900000000000448009

XE2eb

C0795690

900000000000074008

20200731

18735004

Congenital omphalocele

6011000124106~MAPADVICE~IF LETHAL OMPHALOCELE WITH CLEFT PALATE SYNDROME CHOOSE Q79.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~Q79.0

6011000124106~MAPRULE~IFA 196856007 | Omphalocele with gangrene (disorder) |

447562003~MAPTARGET~K76.9

6011000124106~MAPTARGET~K76.9

447562003~MAPRULE~TRUE

6011000124106~MAPADVICE~IF LETHAL OMPHALOCELE WITH CLEFT PALATE SYNDROME CHOOSE Q35.9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF BECKWITH-WIEDEMANN SYNDROME CHOOSE Q87.3 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPADVICE~IF HEPATOMPHALOCELE CHOOSE K76.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~7

6011000124106~MAPPRIORITY~4

6011000124106~MAPTARGET~Q35.9

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

6011000124106~MAPTARGET~Q87.0

6011000124106~MAPADVICE~IF HEPATOMPHALOCELE CHOOSE Q79.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~

6011000124106~MAPCATEGORYID~447638001

6011000124106~MAPGROUP~1

6011000124106~MAPGROUP~2

447562003~MAPGROUP~2

447562003~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA

6011000124106~MAPRULE~IFA 196856007 | Omphalocele with gangrene |

6011000124106~MAPADVICE~IF CONGENITAL OMPHALOCELE, DIAPHRAGMATIC HERNIA, CARDIOVASCULAR ANOMALIES, RADIAL RAY DEFECT SYNDROME CHOOSE Q79.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPADVICE~IF BECKWITH-WIEDEMANN SYNDROME CHOOSE Q87.3 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000508004~ACCEPTABILITYID~900000000000549004

6011000124106~MAPRULE~IFA 36631002 | Hepatomphalocele |

447562003~MAPGROUP~1

900000000000497000~MAPTARGET~XE2eb

6011000124106~MAPTARGET~K42.1

447562003~CORRELATIONID~447561005

6011000124106~MAPRULE~IFA 719408007 | Lethal omphalocele with cleft palate syndrome (disorder) |

447562003~MAPRULE~OTHERWISE TRUE

447562003~MAPRULE~IFA 81780002 | Beckwith-Wiedemann syndrome (disorder) |

6011000124106~MAPCATEGORYID~447637006

6011000124106~MAPTARGET~Q79.2

447562003~MAPTARGET~Q79.2

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPRULE~IFA 1172589000 | Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome |

447562003~MAPADVICE~IF OMPHALOCELE WITH OBSTRUCTION CHOOSE K56.6 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF CONGENITAL OMPHALOCELE, DIAPHRAGMATIC HERNIA, CARDIOVASCULAR ANOMALIES, RADIAL RAY DEFECT SYNDROME CHOOSE Q74.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000508004~ACCEPTABILITYID~900000000000548007

447562003~MAPTARGET~

447562003~MAPTARGET~K56.6

6011000124106~MAPTARGET~Q87.3

447562003~MAPPRIORITY~1

6011000124106~MAPRULE~IFA 81780002 | Beckwith-Wiedemann syndrome (disorder) |

447562003~MAPCATEGORYID~447637006

6011000124106~MAPTARGET~Q28.9

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPRULE~IFA 36631002 | Hepatomphalocele (disorder) |

6011000124106~MAPPRIORITY~5

6011000124106~MAPADVICE~IF FAMILIAL OMPHALOCELE SYNDROME WITH FACIAL DYSMORPHISM CHOOSE Q79.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPGROUP~4

6011000124106~MAPTARGET~Q74.0

6011000124106~MAPCATEGORYID~447639009

447562003~MAPRULE~IFA 1542009 | Omphalocele with obstruction (disorder) |

6011000124106~MAPADVICE~IF CONGENITAL OMPHALOCELE, DIAPHRAGMATIC HERNIA, CARDIOVASCULAR ANOMALIES, RADIAL RAY DEFECT SYNDROME CHOOSE Q28.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPADVICE~ALWAYS Q79.2

447562003~MAPPRIORITY~3

6011000124106~MAPRULE~IFA 719408007 | Lethal omphalocele with cleft palate syndrome |

447562003~MAPCATEGORYID~447639009

6011000124106~MAPPRIORITY~1

6011000124106~MAPADVICE~IF HEPATOMPHALOCELE CHOOSE K76.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~6

6011000124106~MAPRULE~IFA 770900000 | Familial omphalocele syndrome with facial dysmorphism |

447562003~MAPTARGET~Q87.3

6011000124106~CORRELATIONID~447561005

6011000124106~MAPADVICE~ALWAYS Q79.2

6011000124106~MAPADVICE~IF OMPHALOCELE WITH GANGRENE CHOOSE K42.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPRULE~IFA 36631002 | Hepatomphalocele (disorder) |

447562003~MAPPRIORITY~2

6011000124106~MAPGROUP~3

6011000124106~MAPPRIORITY~3

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPPRIORITY~2

447562003~MAPCATEGORYID~447638001

6011000124106~MAPRULE~IFA 81780002 | Beckwith-Wiedemann syndrome |

6011000124106~MAPADVICE~IF FAMILIAL OMPHALOCELE SYNDROME WITH FACIAL DYSMORPHISM CHOOSE Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF CONGENITAL OMPHALOCELE, DIAPHRAGMATIC HERNIA, CARDIOVASCULAR ANOMALIES, RADIAL RAY DEFECT SYNDROME CHOOSE Q79.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

T019

900000000000003001

900000000000013009