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697899000: Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation (disorder)


Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2968120014 Heritable pulmonary arterial hypertension due to BMPR2 mutation en Synonym Active Initial character case insensitive SNOMED CT core
3008434016 Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3008454015 Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II 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 BMPR2 mutation Is a Heritable pulmonary arterial hypertension true Inferred relationship Some
Heritable pulmonary arterial hypertension due to BMPR2 mutation Finding site Pulmonary artery structure true Inferred relationship Some 1
Heritable pulmonary arterial hypertension due to BMPR2 mutation Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Heritable pulmonary arterial hypertension due to BMPR2 mutation Is a Cardiovascular system hereditary disorder true Inferred relationship Some

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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