mitochondrial complex III deficiency nuclear type 6
Human disease
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mitochondrial complex III deficiency nuclear type 6
Summary
mitochondrial complex III deficiency nuclear type 6 is a rare disease[1].
Key Facts
- mitochondrial complex III deficiency nuclear type 6's instance of is recorded as rare disease[2].
- mitochondrial complex III deficiency nuclear type 6's instance of is recorded as class of disease[3].
- mitochondrial complex III deficiency nuclear type 6's subclass of is recorded as mitochondrial complex III deficiency[4].
- mitochondrial complex III deficiency nuclear type 6's subclass of is recorded as genetic disease[5].
- mitochondrial complex III deficiency nuclear type 6's OMIM ID is recorded as 615453[6].
- mitochondrial complex III deficiency nuclear type 6's Disease Ontology ID is recorded as DOID:0080115[7].
- mitochondrial complex III deficiency nuclear type 6's genetic association is recorded as CYC1[8].
- mitochondrial complex III deficiency nuclear type 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080115[9].
- mitochondrial complex III deficiency nuclear type 6's exact match is recorded as http://identifiers.org/doid/DOID:0080115[10].
- mitochondrial complex III deficiency nuclear type 6's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1460[11].
- mitochondrial complex III deficiency nuclear type 6's UMLS CUI is recorded as C3809553[12].
- mitochondrial complex III deficiency nuclear type 6's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- mitochondrial complex III deficiency nuclear type 6's Mondo ID is recorded as MONDO_0014194[14].
- mitochondrial complex III deficiency nuclear type 6's UniProt disease ID is recorded as DI-03905[15].