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SNOMED CT
Last uploaded:
January 16, 2025
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| Id | http://purl.bioontology.org/ontology/SNOMEDCT/17190001
http://purl.bioontology.org/ontology/SNOMEDCT/17190001
|
|---|---|
| Preferred Name | Congenital diaphragmatic hernia |
| Synonyms |
Congenital diaphragmatic hernia (disorder)
CDH - Congenital diaphragmatic hernia
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
Congenital diaphragmatic hernia (disorder)
CDH - Congenital diaphragmatic hernia
|
|---|---|
| prefLabel |
Congenital diaphragmatic hernia
|
| Type ID |
900000000000003001
900000000000013009
|
| CASE SIGNIFICANCE ID |
900000000000020002
900000000000448009
900000000000017005
|
| notation |
17190001
|
| Effective time |
20140731
|
| Active |
1
|
| Has finding site | |
| Has pathological process | |
| Associated finding of | |
| subClassOf | |
| Semantic type UMLS property | |
| Focus of |
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|
| type | |
| Subset member |
6011000124106~MAPTARGET~Q79.0
6011000124106~MAPRULE~IFA 1172705006 | Lethal hydranencephaly, diaphragmatic hernia syndrome |
6011000124106~MAPRULE~IFA 1197754004 | Congenital brachyesophagus, intrathoracic stomach, vertebral anomalies syndrome |
447562003~MAPRULE~TRUE
6011000124106~MAPRULE~IFA 1217373008 | Diaphragmatic hernia, short bowel, asplenia syndrome |
6011000124106~MAPADVICE~IF PERICARDIAL AND DIAPHRAGMATIC DEFECT SYNDROME CHOOSE Q24.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~Q40.2
6011000124106~MAPADVICE~IF DIAPHRAGMATIC DEFECT, LIMB DEFICIENCY, SKULL DEFECT SYNDROME CHOOSE Q79.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~7
6011000124106~MAPPRIORITY~4
6011000124106~MAPADVICE~IF FRYNS SYNDROME CHOOSE Q79.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
6011000124106~MAPTARGET~Q87.0
6011000124106~MAPTARGET~
6011000124106~MAPCATEGORYID~447638001
6011000124106~MAPRULE~IFA 47028006 | Congenital hiatus hernia |
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
6011000124106~MAPPRIORITY~8
447562003~MAPTARGET~Q79.0
900000000000508004~ACCEPTABILITYID~900000000000549004
447562003~MAPGROUP~1
6011000124106~MAPRULE~IFA 721095007 | Diaphragmatic defect, limb deficiency, skull defect syndrome |
6011000124106~MAPTARGET~Q79.1
447562003~CORRELATIONID~447561005
6011000124106~MAPTARGET~Q24.8
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPTARGET~Q04.3
6011000124106~MAPRULE~IFA 724068001 | Pericardial and diaphragmatic defect syndrome |
6011000124106~MAPTARGET~Q74.9
6011000124106~MAPADVICE~IF DIAPHRAGMATIC DEFECT, LIMB DEFICIENCY, SKULL DEFECT SYNDROME CHOOSE Q75.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPADVICE~ALWAYS Q79.0
900000000000508004~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~IF DIAPHRAGMATIC HERNIA, SHORT BOWEL, ASPLENIA SYNDROME CHOOSE Q43.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF DIAPHRAGMATIC HERNIA, SHORT BOWEL, ASPLENIA SYNDROME CHOOSE Q89.01 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~ALWAYS Q79.0
6011000124106~MAPTARGET~Q89.01
447562003~MAPPRIORITY~1
6011000124106~MAPADVICE~IF CONGENITAL BRACHYESOPHAGUS, INTRATHORACIC STOMACH, VERTEBRAL ANOMALIES SYNDROME CHOOSE Q76.49 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPCATEGORYID~447637006
6011000124106~MAPTARGET~Q75.9
6011000124106~MAPRULE~OTHERWISE TRUE
6011000124106~MAPPRIORITY~5
6011000124106~MAPRULE~IFA 702432006 | Fryns syndrome |
6011000124106~MAPADVICE~IF CONGENITAL BRACHYESOPHAGUS, INTRATHORACIC STOMACH, VERTEBRAL ANOMALIES SYNDROME CHOOSE Q39.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPTARGET~Q43.8
6011000124106~MAPTARGET~Q76.49
6011000124106~MAPPRIORITY~1
6011000124106~MAPTARGET~Q39.8
6011000124106~MAPADVICE~IF FRYNS SYNDROME CHOOSE Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~6
6011000124106~MAPADVICE~IF DIAPHRAGMATIC DEFECT, LIMB DEFICIENCY, SKULL DEFECT SYNDROME CHOOSE Q74.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~CORRELATIONID~447561005
6011000124106~MAPADVICE~IF PERICARDIAL AND DIAPHRAGMATIC DEFECT SYNDROME CHOOSE Q79.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~Q74.8
6011000124106~MAPRULE~TRUE
6011000124106~MAPADVICE~IF CONGENITAL BRACHYESOPHAGUS, INTRATHORACIC STOMACH, VERTEBRAL ANOMALIES SYNDROME CHOOSE Q40.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPGROUP~3
6011000124106~MAPPRIORITY~3
6011000124106~MAPTARGET~Q40.1
900000000000509007~ACCEPTABILITYID~900000000000549004
6011000124106~MAPPRIORITY~2
6011000124106~MAPADVICE~IF FRYNS SYNDROME CHOOSE Q74.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF DIAPHRAGMATIC HERNIA, SHORT BOWEL, ASPLENIA SYNDROME CHOOSE Q79.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF LETHAL HYDRANENCEPHALY, DIAPHRAGMATIC HERNIA SYNDROME CHOOSE Q79.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
900000000000497000~MAPTARGET~XE1MG
6011000124106~MAPADVICE~IF LETHAL HYDRANENCEPHALY, DIAPHRAGMATIC HERNIA SYNDROME CHOOSE Q04.3 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF CONGENITAL HIATUS HERNIA CHOOSE Q40.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
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|
| DEFINITION STATUS ID |
900000000000073002
|
| tui |
T019
|
| CTV3ID |
XE1MG
|
| Occurs in | |
| cui |
C0235833
|
| Has associated morphology |
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