mitochondrial complex III deficiency nuclear type 1
Human disease
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mitochondrial complex III deficiency nuclear type 1
Summary
mitochondrial complex III deficiency nuclear type 1 is a developmental defect during embryogenesis[1].
Key Facts
- mitochondrial complex III deficiency nuclear type 1's instance of is recorded as developmental defect during embryogenesis[2].
- mitochondrial complex III deficiency nuclear type 1's instance of is recorded as rare disease[3].
- mitochondrial complex III deficiency nuclear type 1's instance of is recorded as class of disease[4].
- mitochondrial complex III deficiency nuclear type 1 is a type of mitochondrial complex III deficiency[5].
- mitochondrial complex III deficiency nuclear type 1 is a type of mitochondrial disorder due to a defect in assembly or maturation of the respiratory chain complexes[6].
- mitochondrial complex III deficiency nuclear type 1 is a type of genetic disease[7].
- mitochondrial complex III deficiency nuclear type 1's genetic association is recorded as BCS1L[8].
- mitochondrial complex III deficiency nuclear type 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080111[9].
- mitochondrial complex III deficiency nuclear type 1's exact match is recorded as http://identifiers.org/doid/DOID:0080111[10].
- mitochondrial complex III deficiency nuclear type 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_254902[11].
- mitochondrial complex III deficiency nuclear type 1's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].