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766251006: Lethal infantile mitochondrial myopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3661250017 Lethal infantile mitochondrial myopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3661251018 Lethal infantile mitochondrial myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
3661252013 Lethal infantile mitochondrial disease 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
Lethal infantile mitochondrial myopathy Is a Mitochondrial myopathy true Inferred relationship Existential restriction modifier
Lethal infantile mitochondrial myopathy Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Lethal infantile mitochondrial myopathy Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Lethal infantile mitochondrial myopathy Is a Disorder of mitochondrial respiratory chain complexes true Inferred relationship Existential restriction modifier
Lethal infantile mitochondrial myopathy Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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