All individuals with variants in gene GALT

23 entries on 1 page. Showing entries 1 - 23.
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00000062 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000073 - PubMed: Bell 2011 - - - - - - - - - - - 2 1 Global Variome, with Curator vacancy
00080877 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - GALAC1 Galactosemia (OMIM:230400) 1 1 Daniel Trujillano
00211194 Patient 1 PubMed: Estrada, Canson and Silao 2013 - M - Philippines - - - - - GALAC1 Jaundice (HP:0000952) Sepsis (HP:0100806) Hepatomegaly (HP:0002240) 2 1 Daffodil Canson
00211196 Patient 3 PubMed: Estrada, Canson and Silao 2013 - M - Philippines - - - - - GALAC1 Jaundice (HP:0000952), diarrhea (HP:0002014), seizures (HP:0001250), irritability (HP:0000737), poor suck (HP:0002033), sepsis (HP:0100806), hepatomegaly (HP:0002240) 1 1 Daffodil Canson
00213100 24045215-Pat4 PubMed: Estrada 2013 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Philippines - 00y01m - - - GALAC1 5d-jaundice, vomiting, diarrhea; 1m-died due to sepsis 1 1 Johan den Dunnen
00213101 24045215-Pat2 PubMed: Estrada 2013 - M - Philippines - - - - gal-free diet GALAC1 5d-vomiting, diarrhea, jaundice; 1m-hepatomegaly, failure to thrive, sepsis; 2y6m-development and liver function were normal 1 1 Johan den Dunnen
00218060 Patient 2 PubMed: Estrada, Canson and Silao 2013 - M - Philippines - - - - - GALAC1 Vomiting (HP:0002013), diarrhea (HP:0002014), jaundice (HP:0000952), hepatomegaly (HP:0002240), failure to thrive (HP:0001508), sepsis (HP:0100806) 1 1 Daffodil Canson
00218062 Patient 4 PubMed: Estrada, Canson and Silao 2013 - F - Philippines - - - - - GALAC1 Vomiting (HP:0002013), diarrhea (HP:0002014), jaundice (HP:0000952), sepsis (HP:0100806) 1 1 Daffodil Canson
00294849 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00294850 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00294851 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00294852 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00294853 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00294854 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00295229 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00387750 M280 PubMed: Hu 2019 family, 2 affected individuals - - Iran Persia - - - - ID syndromic intellectual disability, no microcephaly, leukoencephalopathy 1 2 Johan den Dunnen
00410547 Pat9 PubMed: Schuermans 2022 analysis 329 adult patients suffering from undiagnosed rare disease F - Belgium - - - - - ? see paper; ..., onset neonatal, intellectual disability, tremor, dyspraxia, hypogonadotropic hypogonadism, no family history 1 1 Johan den Dunnen
00414704 NA01210 PubMed: Bell 2011 - ? - - - - - - - retinal disease - 1 1 LOVD
00428032 A220 PubMed: Bournazos 2022 family, 1 affected - - Australia - - - - - ? - 1 1 Johan den Dunnen
00444973 13DG2254 PubMed: Patel 2017 simplex case - - - - - - - - CTRCT pediatric cataract; not syndromic, clinical signs of galactosemia 1 1 Johan den Dunnen
00445043 ? PubMed: Kessel 2021 patient - - Denmark - - - - - CTRCT bilateral cataract, galactosemia 1 1 Johan den Dunnen
00445072 ? PubMed: Kessel 2021 patient - - Denmark - - - - - CTRCT bilateral cataract, galactosemia 1 1 Johan den Dunnen
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