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SNOMED CT
Last uploaded:
January 16, 2025
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Id | http://purl.bioontology.org/ontology/SNOMEDCT/704241002
http://purl.bioontology.org/ontology/SNOMEDCT/704241002
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Preferred Name | Fetal hypertrophic cardiomyopathy due to maternal diabetes mellitus |
Synonyms |
Foetal hypertrophic cardiomyopathy due to maternal diabetes mellitus
Fetal hypertrophic cardiomyopathy due to maternal diabetes mellitus (disorder)
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Type | http://www.w3.org/2002/07/owl#Class |
All Properties
altLabel |
Foetal hypertrophic cardiomyopathy due to maternal diabetes mellitus
Fetal hypertrophic cardiomyopathy due to maternal diabetes mellitus (disorder)
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prefLabel | Fetal hypertrophic cardiomyopathy due to maternal diabetes mellitus
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Type ID |
900000000000003001
900000000000013009
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CASE SIGNIFICANCE ID | 900000000000448009
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notation | 704241002
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Due to | |
Effective time | 20210131
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Active | 1
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Has finding site | |
subClassOf | |
Semantic type UMLS property | |
type | |
Subset member | 447562003~MAPRULE~TRUE
447562003~MAPTARGET~P29.8
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
447562003~MAPGROUP~2
6011000124106~MAPTARGET~O36.8990
900000000000508004~ACCEPTABILITYID~900000000000549004
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000497000~MAPTARGET~XUncB
900000000000509007~ACCEPTABILITYID~900000000000548007
447562003~MAPADVICE~ALWAYS P29.8
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPTARGET~P70.1
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
447562003~MAPADVICE~ALWAYS P70.1
6011000124106~MAPADVICE~ALWAYS O24.919 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | CONSIDER TRIMESTER SPECIFICATION
6011000124106~MAPADVICE~ALWAYS O36.8990 | CONSIDER TRIMESTER SPECIFICATION | CONSIDER WHICH FETUS IS AFFECTED BY THE MATERNAL CONDITION
6011000124106~MAPTARGET~O24.919
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
6011000124106~MAPRULE~TRUE
900000000000509007~ACCEPTABILITYID~900000000000549004
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DEFINITION STATUS ID | 900000000000074008
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tui | T047
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CTV3ID | XUncB
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Occurs in | |
cui | C3875297
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Has associated morphology |
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