All individuals with variants in gene PC

18 entries on 1 page. Showing entries 1 - 18.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00080981 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - Pyruvate carboxylase deficiency Pyruvate carboxylase deficiency (OMIM:266150) 1 1 Daniel Trujillano
00213141 Pat1 PubMed: Coci 2019, Journal: Coci 2019 2-generation family, 1 affected, unaffected heterozygous carrier parents M yes - - - - - - neurodegeneration see paper; ... 1 1 Emanuele Coci
00213143 Pat5 PubMed: Coci 2019, Journal: Coci 2019 2-generation family, 2 affected brothers, unaffected heterozygous carrier parents M no - - - - - - Pyruvate carboxylase deficiency see paper; ... 2 2 Emanuele Coci
00218072 Pat6 PubMed: Coci 2019, Journal: Coci 2019 younger brother M no - - - - - - Pyruvate carboxylase deficiency see paper; ... 2 1 Emanuele Coci
00274163 Pat29 PubMed: Pronicka 2016 2-generation family, 2 affected brothers F - Poland - - - - - ? neonatal onset; mitochondrial disease criteria score 5; muscle biopsy 2 2 Johan den Dunnen
00274196 Pat71 PubMed: Pronicka 2016 no family history M - Poland - - - - - ? deceased; neonatal onset; mitochondrial disease criteria score 5; muscle biopsy 2 1 Johan den Dunnen
00290497 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00290498 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00290499 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00290500 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 57 Mohammed Faruq
00290501 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 13 Mohammed Faruq
00296604 Pat37 PubMed: Taylor 2014 - F - United Kingdom (Great Britain) British - - - - ? muscle affected; central nervous system affected; heart not affected; liver not affected; seizures, congenital lactic acidosis 2 1 Johan den Dunnen
00374339 S-760 PubMed: Ganapathy 2019 - - - India - - - - - ? Global developmental delay, seizures, shock sepsis, metabolic aciduria, hypoglycemia, anemia, thrombocytopenia, nephrocalcinosis and hypervitaminosis 1 1 Johan den Dunnen
00380216 Pat2 PubMed: Coci 2019, Journal: Coci 2019 2-generation family, 1 affected, unaffected heterozygous carrier parents F no Canada Canada-Aboriginal - - - - neurodegeneration see paper; ..., lactic acidosis, generalized hypotonia 1 1 Johan den Dunnen
00380217 Pat3 PubMed: Coci 2019, Journal: Coci 2019 2-generation family, 1 affected, unaffected parents M - - - - - - - neurodegeneration see paper; ... 1 1 Johan den Dunnen
00380218 Pat4 PubMed: Coci 2019, Journal: Coci 2019 2-generation family, 1 affected, unaffected parents M no - - - - - - neurodegeneration see paper; ... 1 1 Johan den Dunnen
00391857 228P - - F no Spain - - - - - CLIFAHDD, IHPRF1 - 2 1 Alejandro Brea-Fernández
00454718 NGSP67 PubMed: Legati 2016 2-generation family, 2 affected sisters, unaffected heterozygous carrier parents F yes - - - - - - mitochondrial pyramidal signs, intellectual disability, leukoencephalopathy 1 2 Daniele Ghezzi
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.