mitochondrial complex V (ATP synthase) deficiency nuclear type 1

mitochondrial complex V (ATP synthase) deficiency nuclear type 1

http://purl.obolibrary.org/obo/DOID_0050768

A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in mutation in the ATPAF2 gene on chromosome 17p11. [ http://purl.obolibrary.org/obo/ECO_0007636 url:http://omim.org/entry/604273 ]

Synonyms: MC5DN1

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This is just here as a test because I lose it

Term information

database cross reference

MIM:604273

Subsets

DO_rare_slim

acronym

MC5DN1

created by

lschriml

creation date

2013-02-21T11:26:46Z

has obo namespace

disease_ontology

DOID:0050768

Term relations

Subclass of:

mitochondrial complex V (ATP synthase) deficiency
disease has basis in some structural_variant