mitochondrial complex V (ATP synthase) deficiency nuclear type 4
mitochondrial metabolism disease that has material basis in mutation in the ATP5A1 gene on chromosome 18q
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Summary
mitochondrial complex V (ATP synthase) deficiency nuclear type 4 is a rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- mitochondrial complex V (ATP synthase) deficiency nuclear type 4's instance of is recorded as rare disease[3].
- mitochondrial complex V (ATP synthase) deficiency nuclear type 4's instance of is recorded as class of disease[4].
- mitochondrial complex V (ATP synthase) deficiency nuclear type 4 is a type of mitochondrial complex V (ATP synthase) deficiency[5].
- mitochondrial complex V (ATP synthase) deficiency nuclear type 4 is a type of genetic disease[6].
- mitochondrial complex V (ATP synthase) deficiency nuclear type 4's genetic association is recorded as ATP5F1A[7].
- mitochondrial complex V (ATP synthase) deficiency nuclear type 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060333[8].
- mitochondrial complex V (ATP synthase) deficiency nuclear type 4's exact match is recorded as http://identifiers.org/doid/DOID:0060333[9].
- mitochondrial complex V (ATP synthase) deficiency nuclear type 4's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_254913[10].
- mitochondrial complex V (ATP synthase) deficiency nuclear type 4's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
Why It Matters
mitochondrial complex V (ATP synthase) deficiency nuclear type 4 is known by 5 alternative names across languages and contexts.[2]