Preferred Name |
Heritable pulmonary arterial hypertension |
|
Synonyms |
Heritable pulmonary arterial hypertension (disorder) |
|
ID |
http://purl.bioontology.org/ontology/SNOMEDCT/697897003 |
|
Active |
1 |
|
altLabel |
Heritable pulmonary arterial hypertension (disorder) |
|
CASE SIGNIFICANCE ID |
900000000000448009 |
|
CTV3ID |
XUmEz |
|
cui |
C0340543 |
|
DEFINITION STATUS ID |
900000000000074008 |
|
Effective time |
20140131 |
|
Has finding site | ||
notation |
697897003 |
|
prefLabel |
Heritable pulmonary arterial hypertension |
|
Subset member |
447562003~MAPRULE~TRUE 6011000124106~MAPADVICE~IF HERITABLE PULMONARY ARTERIAL HYPERTENSION DUE TO ALK1 OR ENDOGLIN MUTATION CHOOSE Q99.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~I27.0 6011000124106~MAPADVICE~IF HERITABLE PULMONARY ARTERIAL HYPERTENSION DUE TO ACTIVIN A RECEPTOR TYPE II-LIKE KINASE 1 OR ENDOGLIN MUTATION CHOOSE Q99.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF BRADDOCK SYNDROME CHOOSE Q87.89 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA 6011000124106~MAPRULE~IFA 720575002 | Braddock syndrome | 6011000124106~MAPRULE~IFA 720575002 | Braddock syndrome (disorder) | 6011000124106~MAPTARGET~ 6011000124106~MAPCATEGORYID~447638001 6011000124106~MAPGROUP~1 6011000124106~MAPGROUP~2 447562003~MAPADVICE~ALWAYS I27.0 6011000124106~MAPADVICE~ALWAYS I27.0 447562003~MAPGROUP~1 6011000124106~MAPTARGET~Q87.89 447562003~CORRELATIONID~447561005 6011000124106~MAPCATEGORYID~447637006 900000000000509007~ACCEPTABILITYID~900000000000548007 900000000000497000~MAPTARGET~XUmEz 6011000124106~MAPADVICE~IF HERITABLE PULMONARY ARTERIAL HYPERTENSION DUE TO ALK1 OR ENDOGLIN MUTATION CHOOSE Q99.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000508004~ACCEPTABILITYID~900000000000548007 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 6011000124106~MAPRULE~IFA 697900005 | Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation | 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPADVICE~IF HERITABLE PULMONARY ARTERIAL HYPERTENSION DUE TO ALK1 OR ENDOGLIN MUTATION CHOOSE I27.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 697900005 | Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation (disorder) | 6011000124106~MAPCATEGORYID~447639009 6011000124106~MAPPRIORITY~1 6011000124106~CORRELATIONID~447561005 447562003~MAPTARGET~I27.0 6011000124106~MAPTARGET~Q99.9 6011000124106~MAPPRIORITY~3 6011000124106~MAPPRIORITY~2 6011000124106~MAPTARGET~Q99.8 |
|
tui |
T047 |
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Type ID |
900000000000003001 900000000000013009 |
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subClassOf |