All individuals with variants in gene G6PC3

6 entries on 1 page. Showing entries 1 - 6.
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AscendingIndividual ID     

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00001636 - PubMed: Lines 2012 - F no - - - - - - MFDGA;MFDM IUGR; Malar hypoplasia; Micrognathia; Upslanting of obliquity of palpebrae; Microtia; Unilateral preauricular tags; Unilateral auditory canal atresia/stenosis; Conductive hearing loss; Midline cleft palate; Moderate to severe global developmental delay; Walking at 24-36m; Congenital heart defect(VSD; 46,XX; no seizures 1 1 Johan den Dunnen
00239630 - - - M - - - - - - - ? HP:0001875 (Neutropenia) 1 1 IMGAG
00291741 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00433113 Pat91,1 PubMed: Stray-Pedersen 2017 3-generation family, 2 affected cousins, unaffected heterozygous carrier relatives M - Mexico - - - - - IMD neutropenia, congenital heart defect 2 2 Johan den Dunnen
00433114 Pat91,4 PubMed: Stray-Pedersen 2017 cousin M - Mexico - - - - - IMD neutropenia, congenital heart defect 1 1 Johan den Dunnen
00433121 Pat98,1 PubMed: Stray-Pedersen 2017 - F - Pakistan - - - - - IMD neutrophil defect or congenital condition with bone marrow failure such as dyskeratosis congenita and Fanconi-like phenotype, anemia and thrombocytopenia 1 1 Johan den Dunnen
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