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703530005: Brody myopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3009048016 Brody myopathy en Synonym Active Entire term case sensitive SNOMED CT core module
3009283012 Brody disease en Synonym Active Entire term case sensitive SNOMED CT core module
3009458010 Brody myopathy (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Brody myopathy Is a Disorder of skeletal muscle true Inferred relationship Existential restriction modifier
Brody myopathy Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Brody myopathy Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Brody 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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