Phenotypes for disease #03079 (COQ10D4;SCAR9 (coenzyme Q10 deficiency, primary, type 4), OMIM:612016)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000060367 Coenzyme Q10 deficiency, primary, 4 (OMIM:612016) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080798
0000060536 Coenzyme Q10 deficiency, primary, 4 (OMIM:612016) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080967
0000060633 Coenzyme Q10 deficiency, primary, 4 (OMIM:612016) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00081064
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