Preferred Name |
Congenital diaphragmatic hernia |
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Synonyms |
Congenital diaphragmatic hernia (disorder) CDH - Congenital diaphragmatic hernia |
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ID |
http://purl.bioontology.org/ontology/SNOMEDCT/17190001 |
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Active |
1 |
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altLabel |
Congenital diaphragmatic hernia (disorder) CDH - Congenital diaphragmatic hernia |
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Associated finding of |
http://purl.bioontology.org/ontology/SNOMEDCT/6900001000004102 |
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CASE SIGNIFICANCE ID |
900000000000020002 900000000000448009 900000000000017005 |
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CTV3ID |
XE1MG |
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cui |
C0235833 |
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DEFINITION STATUS ID |
900000000000073002 |
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Effective time |
20140731 |
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Focus of | ||
Has associated morphology | ||
Has finding site | ||
Has pathological process | ||
notation |
17190001 |
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Occurs in | ||
prefLabel |
Congenital diaphragmatic hernia |
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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 |
|
tui |
T019 |
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Type ID |
900000000000003001 900000000000013009 |
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subClassOf |