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732245008: Pure mitochondrial myopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3464493014 Pure mitochondrial myopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3464494015 Pure mitochondrial myopathy 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
Pure mitochondrial myopathy Is a Mitochondrial myopathy true Inferred relationship Existential restriction modifier
Pure mitochondrial myopathy Is a Congenital disease true Inferred relationship Existential restriction modifier
Pure mitochondrial myopathy Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Pure mitochondrial myopathy Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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