All individuals with variants in gene MTO1

16 entries on 1 page. Showing entries 1 - 16.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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VIP     

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Panel size     

Owner     
00001574 - - - F yes - - - - - - - - 1 2 Daniele Ghezzi
00001575 - - - F no Italy - - - - - - - 1 1 Daniele Ghezzi
00036287 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036288 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036289 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036290 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00050621 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected parents M - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay, aggressive behavior, restrictive behavior, microcephaly, abnormal facial shape, macrotia, abnormality of eye movement 1 2 Johan den Dunnen
00100427 - - - M no Netherlands - - - - - CMH - 2 1 Rick Kamps
00150179 26539891-FamBAB4863 PubMed: Karaca 2015 - - - - - - - family structure in paper - ? hydrocephaly, dysgenesis of corpus callosum 2 1 Johan den Dunnen
00296579 Pat12 PubMed: Kemp 2011, PubMed: Taylor 2014 - F - Croatia (Hrvatska) - - - - - ? muscle affected; central nervous system affected; heart affected; liver not affected; lactic acidosis 2 1 Johan den Dunnen
00296580 Pat13 PubMed: Kemp 2011, PubMed: Taylor 2014 - M yes United Kingdom (Great Britain) Pakistan 1y - - - ? deceased; muscle not affected; central nervous system not affected; heart affected; liver not affected; 1 1 Johan den Dunnen
00296581 Pat14 PubMed: Kemp 2011, PubMed: Taylor 2014 - M yes United Kingdom (Great Britain) Pakistan 3y - - - ? deceased; muscle affected; central nervous system affected; heart affected; liver affected; coagulopathy, renal failure, lactic acidosis 1 1 Johan den Dunnen
00296582 Pat15 PubMed: Taylor 2014 - M - United Kingdom (Great Britain) British - - - - ? muscle affected; central nervous system not affected; heart not affected; liver not affected; lactic acidosis 2 1 Johan den Dunnen
00315502 SUDS084 PubMed: Neubauer 2021 - M - Switzerland Europe 07y - - - SUD SUD 1 1 Cordula Haas
00430266 213046 - - M yes Turkey - - - - - COXPD10 Neurodevelopmental delay, Motor delay, Decreased activity of mitochondrial complex IV, Decreased activity of mitochondrial complex I, Hypertrophic cardiomyopathy, Intellectual disability, mild, Increased serum lactate 1 1 Andreas Laner
00457789 - - - F - - (not applicable) white - - - - CMD HP:0001644 2 1 Marketa Wayhelova
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