Disease #00606 (mitochondrial respiratory chain complex II deficiency, OMIM:252011)

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Official abbreviation	-
Name	mitochondrial respiratory chain complex II deficiency
OMIM ID	252011
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 3 genes	SDHA, SDHAF1, SDHD
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A