FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

237995002: Depletion of mitochondrial deoxyribonucleic acid (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
356709010 Depletion of mitochondrial DNA en Synonym Active Only initial character case insensitive SNOMED CT core module
2970105015 Depletion of mitochondrial deoxyribonucleic acid en Synonym Active Entire term case insensitive SNOMED CT core module
2970736019 Depletion of mitochondrial deoxyribonucleic acid (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

14 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Depletion of mitochondrial deoxyribonucleic acid Is a Disorder of mitochondrial respiratory chain complexes true Inferred relationship Existential restriction modifier
Depletion of mitochondrial deoxyribonucleic acid Finding site Body system structure false Inferred relationship Existential restriction modifier
Depletion of mitochondrial deoxyribonucleic acid Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Myoclonic epilepsy myopathy sensory ataxia Is a True Depletion of mitochondrial deoxyribonucleic acid Inferred relationship Existential restriction modifier
TK2-related mitochondrial deoxyribonucleic acid depletion syndrome myopathic form Is a False Depletion of mitochondrial deoxyribonucleic acid Inferred relationship Existential restriction modifier
Fatal infantile lactic acidosis co-occurrent with methylmalonic aciduria Is a False Depletion of mitochondrial deoxyribonucleic acid Inferred relationship Existential restriction modifier
Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency Is a True Depletion of mitochondrial deoxyribonucleic acid Inferred relationship Existential restriction modifier
Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form Is a True Depletion of mitochondrial deoxyribonucleic acid Inferred relationship Existential restriction modifier
Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form Is a True Depletion of mitochondrial deoxyribonucleic acid Inferred relationship Existential restriction modifier
Recessive mitochondrial ataxia syndrome Is a True Depletion of mitochondrial deoxyribonucleic acid Inferred relationship Existential restriction modifier
Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency Is a True Depletion of mitochondrial deoxyribonucleic acid Inferred relationship Existential restriction modifier
Navajo neurohepatopathy Is a True Depletion of mitochondrial deoxyribonucleic acid Inferred relationship Existential restriction modifier
Mitochondrial deoxyribonucleic acid depletion syndrome myopathic form Is a True Depletion of mitochondrial deoxyribonucleic acid Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start