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


Status: current, Primitive. 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 Active Initial character case insensitive 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 Initial character case insensitive SNOMED CT core
3008496016 Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation en Synonym Active Initial character case insensitive SNOMED CT core
3008507016 Heritable pulmonary arterial hypertension due to ACVRL1 or endoglin mutation en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

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

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

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