All individuals with variants in gene ADCK3

15 entries on 1 page. Showing entries 1 - 15.
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00080798 - PubMed: Trujillano 2017 unaffected heterozygous carrier mother - - - - - - - - COQ10D4;SCAR9 Coenzyme Q10 deficiency, primary, 4 (OMIM:612016) 2 1 Daniel Trujillano
00080967 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - COQ10D4;SCAR9 Coenzyme Q10 deficiency, primary, 4 (OMIM:612016) 1 1 Daniel Trujillano
00081064 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - COQ10D4;SCAR9 Coenzyme Q10 deficiency, primary, 4 (OMIM:612016) 1 1 Daniel Trujillano
00154963 - - - F - (Germany) - - - - - ? Limb ataxia (HP:0002070); Gait ataxia (HP:0002066); Cerebellar atrophy (HP:0001272) 2 1 IMGAG
00181151 41637 - - M no Switzerland - - - - - EE - 2 1 Anaïs Begemann
00207944 - - - M - Germany - - - - - - HP:0012638 (Abnormality of nervous system physiology); HP:0003201 (Rhabdomyolysis); HP:0100753 (Schizophrenia); HP:0011805 (Abnormality of muscle morphology) 1 1 Andreas Laner
00225676 25558065-Fam09DG00930 PubMed: Alazami 2015, Journal: Alazami 2015 - - yes Saudi Arabia - - - - - ? see paper; …, isolated cerebellar hypoplasia 1 1 Johan den Dunnen
00265599 - - - F - - - - - - - ? Ataxia (HP:0001251); Intellectual disability, mild (HP:0001256) 1 1 IMGAG
00274189 Pat61 PubMed: Pronicka 2016 no family history M - Poland - - - - - ? deceased; mitochondrial disease criteria score 8; muscle biopsy 2 1 Johan den Dunnen
00289745 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 58 Mohammed Faruq
00307150 Pat9 PubMed: Krygier 2019 2-generation family, affected male twins, unaffected heterozygous carrier parents M - Poland - - - - - ataxia generalized dystonia, tremor, cognitive decline, increased serum lactate; MRI brain cerebellar atrophy 2 2 Johan den Dunnen
00375643 Pat18 PubMed: Srivastava 2014 - - - United States - - - - - ? progressive; intellectual disability/developmental delay; seizures; dysarthria; hypotonia, tremor, ataxia, dysmetria, broad-based gait; MRI brain cerebellar atrophy 2 1 Johan den Dunnen
00431865 SIDS022 - - F - Switzerland Europe 00y09m - - - SIDS SIDS 1 1 Cordula Haas
00440358 Pat42;PED2037.1 PubMed: Thevenon 2016, PubMed: Nambot 2018 - M - France - - - - - NDD epilepsy; epileptic encephalopathy 2 1 Johan den Dunnen
00440454 PED3374.1 PubMed: Nambot 2018 - - - France - - - - - ? - 2 1 Johan den Dunnen
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