mitochondrial complex V (ATP synthase) deficiency, nuclear type 1
mitochondrial metabolism disease that has material basis in mutation in the ATPAF2 gene on chromosome 17p11
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Summary
mitochondrial complex V (ATP synthase) deficiency, nuclear type 1 is a rare disease[1]. It is known by 6 alternative names across languages and contexts.[2]
Key Facts
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 1's instance of is recorded as rare disease[3].
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 1's instance of is recorded as class of disease[4].
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 1 is a type of mitochondrial complex V (ATP synthase) deficiency[5].
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 1 is a type of genetic disease[6].
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 1's genetic association is recorded as ATPAF2[7].
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050768[8].
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 1's exact match is recorded as http://identifiers.org/doid/DOID:0050768[9].
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_254913[10].
- mitochondrial complex V (ATP synthase) deficiency, nuclear type 1's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
Why It Matters
mitochondrial complex V (ATP synthase) deficiency, nuclear type 1 is known by 6 alternative names across languages and contexts.[2]