mitochondrial complex III deficiency nuclear type 7
mitochondrial complex III deficiency that has material basis in homozygous mutation in the UQCC2 gene on chromosome 6p21
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mitochondrial complex III deficiency nuclear type 7
Summary
mitochondrial complex III deficiency nuclear type 7 is a rare disease[1]. It is known by 4 alternative names across languages and contexts.[2]
Key Facts
- mitochondrial complex III deficiency nuclear type 7's instance of is recorded as rare disease[3].
- mitochondrial complex III deficiency nuclear type 7's instance of is recorded as class of disease[4].
- mitochondrial complex III deficiency nuclear type 7 is a type of mitochondrial complex III deficiency[5].
- mitochondrial complex III deficiency nuclear type 7 is a type of genetic disease[6].
- mitochondrial complex III deficiency nuclear type 7's genetic association is recorded as UQCC2[7].
- mitochondrial complex III deficiency nuclear type 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080116[8].
- mitochondrial complex III deficiency nuclear type 7's exact match is recorded as http://identifiers.org/doid/DOID:0080116[9].
- mitochondrial complex III deficiency nuclear type 7's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1460[10].
- mitochondrial complex III deficiency nuclear type 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
Why It Matters
mitochondrial complex III deficiency nuclear type 7 is known by 4 alternative names across languages and contexts.[2]