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1208621008: Multiple mitochondrial dysfunctions syndrome type 4 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Mar 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4965432011 Multiple mitochondrial dysfunctions syndrome type 4 en Synonym Active Entire term case insensitive SNOMED CT core module
4965433018 MMDS4 - multiple mitochondrial dysfunctions syndrome type 4 en Synonym Active Entire term case sensitive SNOMED CT core module
4965434012 Multiple mitochondrial dysfunctions syndrome type 4 (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
Multiple mitochondrial dysfunctions syndrome type 4 Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
Multiple mitochondrial dysfunctions syndrome type 4 Is a Inherited metabolic disorder of nervous system true Inferred relationship Existential restriction modifier
Multiple mitochondrial dysfunctions syndrome type 4 Is a Chronic nervous system disorder true Inferred relationship Existential restriction modifier
Multiple mitochondrial dysfunctions syndrome type 4 Is a Chronic metabolic disorder true Inferred relationship Existential restriction modifier
Multiple mitochondrial dysfunctions syndrome type 4 Is a Leukodystrophy true Inferred relationship Existential restriction modifier
Multiple mitochondrial dysfunctions syndrome type 4 Is a Inherited optic neuropathy true Inferred relationship Existential restriction modifier
Multiple mitochondrial dysfunctions syndrome type 4 Is a Multiple mitochondrial dysfunctions syndrome true Inferred relationship Existential restriction modifier
Multiple mitochondrial dysfunctions syndrome type 4 Clinical course Progressive true Inferred relationship Existential restriction modifier 4
Multiple mitochondrial dysfunctions syndrome type 4 Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Multiple mitochondrial dysfunctions syndrome type 4 Finding site Optic nerve structure true Inferred relationship Existential restriction modifier 5
Multiple mitochondrial dysfunctions syndrome type 4 Finding site Myelinated nerve fiber structure true Inferred relationship Existential restriction modifier 1
Multiple mitochondrial dysfunctions syndrome type 4 Associated morphology Myelin sheath alteration true Inferred relationship Existential restriction modifier 1
Multiple mitochondrial dysfunctions syndrome type 4 Finding site White matter structure of brain and spinal cord true Inferred relationship Existential restriction modifier 2
Multiple mitochondrial dysfunctions syndrome type 4 Associated morphology Dystrophy 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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