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1222644009: Autosomal dominant mitochondrial myopathy with exercise intolerance (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
5048276010 Autosomal dominant mitochondrial myopathy with exercise intolerance en Synonym Active Entire term case insensitive SNOMED CT core module
5048277018 Autosomal dominant mitochondrial myopathy with exercise intolerance (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant mitochondrial myopathy with exercise intolerance Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant mitochondrial myopathy with exercise intolerance Is a Chronic disease of musculoskeletal system true Inferred relationship Existential restriction modifier
Autosomal dominant mitochondrial myopathy with exercise intolerance Is a Chronic metabolic disorder true Inferred relationship Existential restriction modifier
Autosomal dominant mitochondrial myopathy with exercise intolerance Is a Mitochondrial myopathy true Inferred relationship Existential restriction modifier
Autosomal dominant mitochondrial myopathy with exercise intolerance Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Autosomal dominant mitochondrial myopathy with exercise intolerance Clinical course Progressive true Inferred relationship Existential restriction modifier 1
Autosomal dominant mitochondrial myopathy with exercise intolerance Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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