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Metadata
ID DOID:0060332
Name mitochondrial complex V (ATP synthase) deficiency nuclear type 3
Definition A mitochondrial complex V (ATP synthase) deficiency that has material basis in mutation in the ATP5E gene on chromosome 20q13.
http://omim.org/entry/614053
Xrefs

ICD10CM:E88.8

OMIM:614053

ORDO:254913

Subsets

DO_rare_slim

Synonyms

MC5DN3 [EXACT]

Parent Relationships

is_a mitochondrial complex V (ATP synthase) deficiency

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