Disease #00606

Official abbreviation -
Name mitochondrial respiratory chain complex II deficiency
OMIM ID 252011
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 3 genes SDHA, SDHAF1, SDHD
Associated tissues -
Disease features -
Remarks -

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