Coenzyme Q10 Deficiency

Preferred Label : Coenzyme Q10 Deficiency;

NCIt definition : A genetically heterogeneous condition, typically inherited in an autosomal recessive fashion, characterized by coenzyme Q10 deficiency.;

Details

Origin ID

C142083;

UMLS CUI

C1843920;

Currated CISMeF NLP mapping
- Coenzyme Q10 deficiency [ORDO Disease]
- Coenzyme Q10 deficiency [ICD-11 Sub-sub category]
- Coenzyme Q10 deficiency (disorder) [SNOMED CT concept]
- coenzyme Q10 deficiency [MeSH Supplementary Concept]
- coenzyme Q10 deficiency [MeSH concept]
- coenzyme Q10 deficiency [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Coenzyme Q10 deficiency [ORDO Disease]
- Coenzyme Q10 deficiency [ICD-11 Sub-sub category]
- Coenzyme Q10 deficiency (disorder) [SNOMED CT concept]
- coenzyme Q10 deficiency [MeSH Supplementary Concept]
- coenzyme Q10 deficiency [MeSH concept]
- coenzyme Q10 deficiency [Disease (Nov.)]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]
may_be_associated_disease_of_disease
- Nephrotic Syndrome - PDSS2 Associated [NCIt concept]

Keyword's position in hierarchy(ies) :

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