697900005: Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of trunk structure\Finding of upper trunk\Disorder of thoracic segment of trunk\Disorder of thorax\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\Finding of trunk structure\Finding of upper trunk\Finding of region of thorax\Pulmonary artery finding\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\Finding of trunk structure\Finding of upper trunk\Finding of region of thorax\Disorder of thorax\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\Finding of trunk structure\Disorder of trunk\Disorder of thoracic segment of trunk\Disorder of thorax\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation

\General finding of soft tissue\Blood vessel finding\Arterial finding\Disorder of artery\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\General finding of soft tissue\Blood vessel finding\Arterial finding\Pulmonary artery finding\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\General finding of soft tissue\Blood vessel finding\Disorder of blood vessel\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\General finding of soft tissue\Blood vessel finding\Disorder of blood vessel\Disorder of artery\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\General finding of soft tissue\Disorder of soft tissue\Disorder of blood vessel\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\General finding of soft tissue\Disorder of soft tissue\Disorder of blood vessel\Disorder of artery\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation

\Cardiovascular finding\Disorder of cardiovascular system\Disorder of blood vessel\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\Cardiovascular finding\Disorder of cardiovascular system\Disorder of blood vessel\Disorder of artery\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\Cardiovascular finding\Blood vessel finding\Arterial finding\Disorder of artery\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\Cardiovascular finding\Blood vessel finding\Arterial finding\Pulmonary artery finding\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\Cardiovascular finding\Blood vessel finding\Disorder of blood vessel\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\Cardiovascular finding\Blood vessel finding\Disorder of blood vessel\Disorder of artery\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation

\Disease\Disorder of body system\Disorder of cardiovascular system\Disorder of blood vessel\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\Disease\Disorder of body system\Disorder of cardiovascular system\Disorder of blood vessel\Disorder of artery\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\Disease\Disorder of trunk\Disorder of thoracic segment of trunk\Disorder of thorax\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\Disease\Disorder of soft tissue\Disorder of blood vessel\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation
\Disease\Disorder of soft tissue\Disorder of blood vessel\Disorder of artery\Pulmonary hypertensive arterial disease\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

2968202012 Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation en Synonym Active Only initial character case insensitive SNOMED CT core module

3008430013 Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

3008496016 Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation en Synonym Active Only initial character case insensitive SNOMED CT core module

3008507016 Heritable pulmonary arterial hypertension due to ACVRL1 or endoglin mutation en Synonym Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation	Is a	Heritable pulmonary arterial hypertension	true	Inferred relationship	Existential restriction modifier
Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation	Finding site	Pulmonary artery structure	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
2968202012	Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3008430013	Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3008496016	Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3008507016	Heritable pulmonary arterial hypertension due to ACVRL1 or endoglin mutation	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module