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)\...
• \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

Expanded Value Set

This concept is not in any reference sets

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