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

Official abbreviation MC1DN31
Name Mi complex I deficiency, nuclear type 31
OMIM ID 618251
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene TIMMDC1
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Individuals

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00412091 199700 - - M no Germany - - - - - MC1DN31 (+) Intellectual disability,(+) Muscle weakness,(+) Hypoplasia of the corpus callosum,(+) Lactic acidosis,(+) Abnormal activity of mitochondrial respiratory chain TIMMDC1 TIMMDC1 2 1 Andreas Laner
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