SNOMED CT

Last uploaded: January 31, 2024
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

http://purl.bioontology.org/ontology/SNOMEDCT/81040000

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

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/11399002

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