Phenotypes for disease #03842 (MC3DN-2 (mitochondrial complex III deficiency, nuclear type 2 (MC3DN-2)), OMIM:615157)

4 entries on 1 page. Showing entries 1 - 4.
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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     
0000092998 see paper; mitochondrial complex III deficiency, … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00117528
0000092999 see paper; mitochondrial complex III deficiency, … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00117529
0000093000 see paper; mitochondrial complex III deficiency, … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00117530
0000093001 see paper; mitochondrial complex III deficiency, … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00117531
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