Clinical and research tests for C2orf6 - Genetic Testing Registry (GTR)

Results: 1 to 5 of 5

Select all conditions on this page	Conditions	Synonyms
Select item 322999	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	Combined oxidative phosphorylation deficiency 1 HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE
Select item 1779083	Combined oxidative phosphorylation deficiency 53	ELBRACHT-ISIKAY SYNDROME GLOBAL DEVELOPMENTAL DELAY, PROGRESSIVE MICROCEPHALY, STRUCTURAL BRAIN ABNORMALITIES, AND AUTOINFLAMMATION
Select item 903495	Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3
Select item 1761843	Spermatogenic failure 48
Select item 1782493	Spermatogenic failure 54

Results: 1 to 5 of 5

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