Disease #00321 (MC5DN2 (mitochondrial complex V (ATP synthase) deficiency, nuclear, type 2 (MC5DN-2)), OMIM:614052)

Official abbreviation MC5DN2
Name mitochondrial complex V (ATP synthase) deficiency, nuclear, type 2 (MC5DN-2)
OMIM ID 614052
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene TMEM70
Associated tissues -
Disease features -
Remarks -
Date created 2014-02-02 22:33:24 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00004542 - - - M ? - white - - - - MC5DN2 - TMEM70 TMEM70 1 1 Robert McFarland
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