SNOMED CT

Last uploaded: January 31, 2024
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Preferred Name

Fetus with hereditary disease
Synonyms

Fetus with hereditary disease (disorder)

Foetus with hereditary disease
ID

http://purl.bioontology.org/ontology/SNOMEDCT/199531009
Active

1
altLabel

Fetus with hereditary disease (disorder)

Foetus with hereditary disease
CASE SIGNIFICANCE ID

900000000000448009
CTV3ID

L252.
cui

C0404615
DEFINITION STATUS ID

900000000000073002
Effective time

20220831
notation

199531009
Occurs in

http://purl.bioontology.org/ontology/SNOMEDCT/303112003
prefLabel

Fetus with hereditary disease
Subset member

6011000124106~MAPRULE~IFA 199533007 | Fetus with hereditary disease - delivered |

6011000124106~MAPTARGET~E26.81

447562003~MAPRULE~TRUE

6011000124106~MAPRULE~IFA 700109009 | Bartter syndrome antenatal type 2 |

6011000124106~MAPADVICE~IF FETUS WITH HEREDITARY DISEASE - DELIVERED CHOOSE O35.2XX0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | CONSIDER WHICH FETUS IS AFFECTED BY THE MATERNAL CONDITION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~7

6011000124106~MAPPRIORITY~4

6011000124106~MAPADVICE~IF FETAL ENCASEMENT SYNDROME CHOOSE O35.8XX0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | CONSIDER WHICH FETUS IS AFFECTED BY THE MATERNAL CONDITION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

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

6011000124106~MAPADVICE~IF FETUS WITH HEREDITARY DISEASE - DELIVERED CHOOSE P96.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~

6011000124106~MAPCATEGORYID~447638001

6011000124106~MAPADVICE~IF BARTTER SYNDROME ANTENATAL TYPE 1 CHOOSE E26.81 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPGROUP~1

6011000124106~MAPGROUP~2

6011000124106~MAPRULE~IFA 199533007 | Fetus with hereditary disease - delivered (disorder) |

6011000124106~MAPTARGET~O36.8990

6011000124106~MAPTARGET~D56.0

6011000124106~MAPADVICE~IF LETHAL FETAL CEREBRORENOGENITOURINARY AGENESIS/HYPOPLASIA SYNDROME CHOOSE O35.8XX0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | CONSIDER WHICH FETUS IS AFFECTED BY THE MATERNAL CONDITION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~8

900000000000497000~MAPTARGET~L252.

6011000124106~MAPTARGET~Z37.9

900000000000508004~ACCEPTABILITYID~900000000000549004

6011000124106~MAPADVICE~IF BARTTER SYNDROME ANTENATAL TYPE 2 CHOOSE E26.81 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPGROUP~1

447562003~CORRELATIONID~447561005

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~IF FETUS WITH HEREDITARY DISEASE - DELIVERED CHOOSE Z37.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~O35.2XX0

900000000000508004~ACCEPTABILITYID~900000000000548007

447562003~MAPPRIORITY~1

6011000124106~MAPTARGET~Q89.7

6011000124106~MAPRULE~IFA 700107006 | Bartter syndrome antenatal type 1 |

447562003~MAPCATEGORYID~447637006

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPPRIORITY~5

6011000124106~MAPTARGET~O35.8XX0

6011000124106~MAPRULE~IFA 5300004 | Hemoglobin Bart's hydrops syndrome |

447562003~MAPTARGET~O35.2

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPADVICE~IF HEMOGLOBIN BART'S HYDROPS SYNDROME CHOOSE D56.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~ALWAYS O35.2XX0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | CONSIDER WHICH FETUS IS AFFECTED BY THE MATERNAL CONDITION

6011000124106~MAPPRIORITY~1

6011000124106~MAPPRIORITY~6

6011000124106~MAPRULE~IFA 721232000 | Hydrolethalus syndrome |

6011000124106~CORRELATIONID~447561005

6011000124106~MAPRULE~IFA 725052002 | Fetal cystic fibrosis |

6011000124106~MAPTARGET~P96.9

6011000124106~MAPRULE~TRUE

6011000124106~MAPPRIORITY~3

447562003~MAPADVICE~ALWAYS O35.2

6011000124106~MAPRULE~IFA 1220575002 | Fetal encasement syndrome |

6011000124106~MAPADVICE~IF FETAL CYSTIC FIBROSIS CHOOSE O36.8990 | CONSIDER TRIMESTER SPECIFICATION | CONSIDER WHICH FETUS IS AFFECTED BY THE MATERNAL CONDITION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPADVICE~IF HYDROLETHALUS SYNDROME CHOOSE Q89.7 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~2

6011000124106~MAPRULE~IFA 1237342004 | Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome |
tui

T033
Type ID

900000000000003001

900000000000013009
subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/70591005

http://purl.bioontology.org/ontology/SNOMEDCT/32895009
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