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

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

  Powered by LOVD v.3.0 Build 27
LOVD software ©2004-2022 Leiden University Medical Center 		There are currently no updates.