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

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000003243 - - - Unknown - - - - - Robert McFarland 00004542
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