Mitochondrial Diabetes

Preferred Label : Mitochondrial Diabetes;

NCIt definition : Diabetes mellitus caused by mutation(s) in mitochondrial DNA.;

NCI Metathesaurus CUI : CL521333;

Détails

Origin ID

C131859;

UMLS CUI

C4330695;

Automatic exact mappings (from CISMeF team)
- Maternally inherited diabetes and deafness [ICD-11 More detail]
- Maternally-inherited diabetes and deafness [ORDO Disease]
Has associated anatomic sites
- Digestive System [NCIt concept]
- Endocrine Gland [NCIt concept]
- Endocrine System [NCIt concept]
- Pancreas [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Endocrinology Terminology [NCIt concept]
disease_has_normal_cell_origin
- Islet Cell [NCIt concept]
disease_has_normal_tissue_origin
- Islet of Langerhans [NCIt concept]
disease_has_primary_anatomic_site
- Digestive System [NCIt concept]
- Endocrine System [NCIt concept]
- Islet of Langerhans [NCIt concept]
- Pancreas [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients