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732245008: Pure mitochondrial myopathy (disorder)


Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3464493014 Pure mitochondrial myopathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3464494015 Pure mitochondrial myopathy en Synonym Active Case insensitive SNOMED CT core
3464495019 A rare mitochondrial disease with characteristics of exclusive skeletal muscle involvement without clinical evidence of other organ involvement. Disease manifestations are progressive limb weakness, proximal limb muscle atrophy and eye muscle anomalies (e.g. ocular motility restriction, ptosis). Patients may present with lactic acidosis, diffuse myalgia and overall fatigability (particularly during/after physical activities), dysphagia and diminished deep tendon reflexes. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pure mitochondrial myopathy Is a Mitochondrial myopathy true Inferred relationship Some
Pure mitochondrial myopathy Is a Congenital disease true Inferred relationship Some
Pure mitochondrial myopathy Occurrence Congenital true Inferred relationship Some 1
Pure mitochondrial myopathy Finding site Skeletal muscle structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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