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775908005: Combined oxidative phosphorylation defect type 17 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3736321019 COXPD17 - combined oxidative phosphorylation defect type 17 en Synonym Active Entire term case sensitive SNOMED CT core module
3736322014 Combined oxidative phosphorylation defect type 17 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3736323016 Combined oxidative phosphorylation defect type 17 en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Combined oxidative phosphorylation defect type 17 Finding site Myocardium structure true Inferred relationship Existential restriction modifier 1
Combined oxidative phosphorylation defect type 17 Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Combined oxidative phosphorylation defect type 17 Is a Hypertrophic mitochondrial cardiomyopathy true Inferred relationship Existential restriction modifier
Combined oxidative phosphorylation defect type 17 Due to Mitochondrial cytopathy true Inferred relationship Existential restriction modifier 2
Combined oxidative phosphorylation defect type 17 Associated morphology Hypertrophy true Inferred relationship Existential restriction modifier 1
Combined oxidative phosphorylation defect type 17 Is a Mitochondrial cytopathy true Inferred relationship Existential restriction modifier
Combined oxidative phosphorylation defect type 17 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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