mitochondrial complex II deficiency
Human disease
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mitochondrial complex II deficiency
Summary
mitochondrial complex II deficiency is a developmental defect during embryogenesis[1].
Key Facts
- mitochondrial complex II deficiency's instance of is recorded as developmental defect during embryogenesis[2].
- mitochondrial complex II deficiency's instance of is recorded as rare disease[3].
- mitochondrial complex II deficiency's instance of is recorded as class of disease[4].
- mitochondrial complex II deficiency is a type of mitochondrial disease[5].
- mitochondrial complex II deficiency is a type of isolated oxidative phosphorylation complex disorder[6].
- mitochondrial complex II deficiency is a type of mitochondrial myopathy[7].
- mitochondrial complex II deficiency is a type of genetic disease[8].
- mitochondrial complex II deficiency's ICD-9-CM is recorded as 277.6[9].
- mitochondrial complex II deficiency's health specialty is recorded as neurology[10].
- mitochondrial complex II deficiency's genetic association is recorded as SDHA[11].
- mitochondrial complex II deficiency's genetic association is recorded as SDHAF1[12].
- mitochondrial complex II deficiency's genetic association is recorded as SDHD[13].
- mitochondrial complex II deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060537[14].
- mitochondrial complex II deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0060537[15].
- mitochondrial complex II deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3208[16].
- mitochondrial complex II deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].