Phenotypes for disease #02528 (CORTRD1 (cortisone reductase deficiency, type 1 (CORTRD-1)), OMIM:604931)

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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     
0000070572 IDD secondary to myopathy, premature adrenarche, skin pigmentation abnormalities; transient glycogen storage on muscle biopsy - - Familial, autosomal recessive - - - - - Johan den Dunnen 00092240
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