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1187517009: Maternally inherited mitochondrial myopathy (disorder)


Status: current, Primitive. Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4674063014 Maternally inherited mitochondrial myopathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4674064015 Maternally inherited mitochondrial myopathy en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Maternally inherited mitochondrial myopathy Is a Mitochondrial myopathy true Inferred relationship Some
Maternally inherited mitochondrial myopathy Due to Mitochondrial cytopathy true Inferred relationship Some 2
Maternally inherited mitochondrial myopathy Finding site Skeletal muscle structure true Inferred relationship Some 1
Maternally inherited mitochondrial myopathy Is a Maternally inherited mitochondrial deoxyribonucleic acid disease true Inferred relationship Some
Maternally inherited mitochondrial myopathy Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Australian dialect reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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