Multiple mitochondrial dysfunctions syndrome 7

Preferred Label : Multiple mitochondrial dysfunctions syndrome 7;

Symbol : MMDS7;

Type : Phenotype, molecular basis known;

Prefixed ID : #620423;

Détails

Origin ID

620423;

UMLS CUI

C5830586;

Genes related to phenotype
- Glycine cleavage system h protein [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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