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


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
2968120014 Heritable pulmonary arterial hypertension due to BMPR2 mutation en Synonym Active Only initial character case insensitive SNOMED CT core module
3008434016 Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3008454015 Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation Is a Heritable pulmonary arterial hypertension true Inferred relationship Existential restriction modifier
Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation Finding site Pulmonary artery structure true Inferred relationship Existential restriction modifier 1
Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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