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1222680009: Combined oxidative phosphorylation defect type 24 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-May 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5048480019 Combined oxidative phosphorylation defect type 24 en Synonym Active Entire term case insensitive SNOMED CT core module
5048481015 Combined oxidative phosphorylation defect type 24 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5048482010 COXPD24 - combined oxidative phosphorylation defect type 24 en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Combined oxidative phosphorylation defect type 24 Is a Mitochondrial cytopathy true Inferred relationship Existential restriction modifier
Combined oxidative phosphorylation defect type 24 Is a Autosomal recessive 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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