Phenotypes for disease #06585 (MC1DN31 (Mi complex I deficiency, nuclear type 31), OMIM:618251)

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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000304107 - - (+) Intellectual disability,(+) Muscle weakness,(+) Hypoplasia of the corpus callosum,(+) Lactic acidosis,(+) Abnormal activity of mitochondrial respiratory chain Unknown 22y - - - Andreas Laner 00412091
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