Phenotypes for disease #03692 (COQ10D6 (coenzyme Q10 deficiency, primary, type 6 (COQ10D-6)), OMIM:614650)

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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     
0000143212 steroid resistant nephrotic syndrome, end stage renal disease, sensorineural deafness steroid resistant nephrotic syndrom COQ10D-6 Familial, autosomal recessive 09y 09y 07y 7y - Güven Toksoy 00180941
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