multiple mitochondrial dysfunctions syndrome

Preferred Label : multiple mitochondrial dysfunctions syndrome;

MeSH note : severe autosomal recessive disorder of systemic energy metabolism, resulting in weakness, respiratory failure, lack of neurologic development, lactic acidosis, and early death;

Détails

Origin ID

C565304;

UMLS CUI

C3502075;

Automatic exact mappings (from CISMeF team)
- Multiple mitochondrial dysfunctions syndrome [ORDO Disease]
- Multiple mitochondrial dysfunctions syndrome [OMIM phenotypic series]
- Multiple mitochondrial dysfunctions syndrome (disorder) [SNOMED CT concept]
- multiple mitochondrial dysfunctions syndrome [DO Concept]
DO Cross reference
- multiple mitochondrial dysfunctions syndrome [DO Concept]
MeSH term(s) associated for indexing
- mitochondrial diseases [MeSH Descriptor]
Record concept(s)
- multiple mitochondrial dysfunctions syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Multiple mitochondrial dysfunctions syndrome (disorder) [SNOMED CT concept]

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

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