697900005: hereditaire pulmonale arteriële hypertensie door mutatie van 'activin A receptor type II-like kinase 1' of endogline (aandoening)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of trunk structure\Finding of upper trunk (finding)\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\Disorder of blood vessels of thorax (disorder)\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\Finding of trunk structure\Finding of upper trunk (finding)\Finding of region of thorax\Pulmonary artery finding\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\Finding of trunk structure\Finding of upper trunk (finding)\Finding of region of thorax\Disorder of thorax (disorder)\Disorder of blood vessels of thorax (disorder)\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\Disorder of blood vessels of thorax (disorder)\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation

\General finding of soft tissue\Blood vessel finding\Arterial finding\Disorder of artery (disorder)\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\General finding of soft tissue\Blood vessel finding\Arterial finding\Pulmonary artery finding\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\General finding of soft tissue\Blood vessel finding\Vascular disorder\Disorder of blood vessels of thorax (disorder)\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\General finding of soft tissue\Blood vessel finding\Vascular disorder\Disorder of artery (disorder)\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\General finding of soft tissue\Disorder of soft tissue\Vascular disorder\Disorder of blood vessels of thorax (disorder)\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\General finding of soft tissue\Disorder of soft tissue\Vascular disorder\Disorder of artery (disorder)\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation

\Cardiovascular finding\Disorder of cardiovascular system (disorder)\Vascular disorder\Disorder of blood vessels of thorax (disorder)\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\Cardiovascular finding\Disorder of cardiovascular system (disorder)\Vascular disorder\Disorder of artery (disorder)\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\Cardiovascular finding\Blood vessel finding\Arterial finding\Disorder of artery (disorder)\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\Cardiovascular finding\Blood vessel finding\Arterial finding\Pulmonary artery finding\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\Cardiovascular finding\Blood vessel finding\Vascular disorder\Disorder of blood vessels of thorax (disorder)\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\Cardiovascular finding\Blood vessel finding\Vascular disorder\Disorder of artery (disorder)\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation

\Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Vascular disorder\Disorder of blood vessels of thorax (disorder)\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Vascular disorder\Disorder of artery (disorder)\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\Disease\Disorder of trunk (disorder)\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\Disorder of blood vessels of thorax (disorder)\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\Disease\Disorder of soft tissue\Vascular disorder\Disorder of blood vessels of thorax (disorder)\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
\Disease\Disorder of soft tissue\Vascular disorder\Disorder of artery (disorder)\Pulmonary hypertensive arterial disease (disorder)\Heritable pulmonary arterial hypertension\Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation

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

Descriptions:

Id Description Lang Type Status Case? Module

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

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 (core metadata concept) SNOMED CT core

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

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

7232351000146116 erfelijke pulmonale arteriële hypertensie door mutatie van 'activin A receptor type II-like kinase 1' of endogline nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

7232361000146118 erfelijke pulmonale arteriële hypertensie door mutatie van ACVRL1 of endogline nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

8013741000146116 erfelijke pulmonale arteriële hypertensie door mutatie van ALK1 of endogline nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

8617991000146114 hereditaire pulmonale arteriële hypertensie door mutatie van 'activin A receptor type II-like kinase 1' of endogline (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

8671821000146116 hereditaire pulmonale arteriële hypertensie door mutatie van 'activin A receptor type II-like kinase 1' of endogline nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation	Is a	Heritable pulmonary arterial hypertension	true	Inferred relationship	Some
Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation	Finding site	Pulmonary artery structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
2968202012	Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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 (core metadata concept)	SNOMED CT core
3008496016	Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3008507016	Heritable pulmonary arterial hypertension due to ACVRL1 or endoglin mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
7232351000146116	erfelijke pulmonale arteriële hypertensie door mutatie van 'activin A receptor type II-like kinase 1' of endogline	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
7232361000146118	erfelijke pulmonale arteriële hypertensie door mutatie van ACVRL1 of endogline	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8013741000146116	erfelijke pulmonale arteriële hypertensie door mutatie van ALK1 of endogline	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8617991000146114	hereditaire pulmonale arteriële hypertensie door mutatie van 'activin A receptor type II-like kinase 1' of endogline (aandoening)	nl	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8671821000146116	hereditaire pulmonale arteriële hypertensie door mutatie van 'activin A receptor type II-like kinase 1' of endogline	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)