All individuals with variants in gene DLD

9 entries on 1 page. Showing entries 1 - 9.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00080796 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - DLDD, MTCO1 Cytochrome c oxidase subunit I (OMIM:516030), Dihydrolipoamide dehydrogenase deficiency (OMIM:246900) 1 1 Daniel Trujillano
00080853 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - DLDD Dihydrolipoamide dehydrogenase deficiency (OMIM:246900) 1 1 Daniel Trujillano
00080986 - PubMed: Trujillano 2017 no information from parents - - - - - - - - DLDD Dihydrolipoamide dehydrogenase deficiency (OMIM:246900) 1 1 Daniel Trujillano
00209013 28771251-Pat16 PubMed: Lionel 2018 - F - Canada - - - - - mitochondrial suspected mitochondrial disorder 1 1 Johan den Dunnen
00266292 - - - M - - - - - - - ? Acute hepatic failure (HP:0006554) 1 1 IMGAG
00274165 Pat31 PubMed: Pronicka 2016 - F - Poland - - - - - ? mitochondrial disease criteria score 6; muscle biopsy 1 1 Johan den Dunnen
00294261 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00294262 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00454708 NGSP33 PubMed: Legati 2016 - F - - - - - - - mitochondrial Leigh syndrome 1 1 Daniele Ghezzi
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