All individuals with variants in gene GLDN

14 entries on 1 page. Showing entries 1 - 14.
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00000208 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), no prolactin deficiency, age sonographic determination testicular volume 17.64y, testicular volume right/left 21/20 (7.3–16ml) 3 1 Yu Sun
00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 1 1 Yu Sun
00105215 Patient_1 Manuscript in submission - - - - - - - - - LCCS11 - 2 1 Dustin Baldridge
00105216 Patient_2 Manuscript in submission - - - - - - - - - LCCS11 - 2 1 Dustin Baldridge
00105217 Patient_3 Manuscript in submission - - - - - - - - - LCCS11 - 2 1 Dustin Baldridge
00105218 Patient_4 Manuscript in submission - - - - - - - - - LCCS11 - 1 1 Dustin Baldridge
00105219 Patient_5 Manuscript in submission - - - - - - - - - LCCS11 - 1 1 Dustin Baldridge
00105220 Patient_6 Manuscript in submission - - - - - - - - - LCCS11 - 1 1 Dustin Baldridge
00105221 Patient_8 Manuscript in submission - - - - - - - - - LCCS11 - 2 1 Dustin Baldridge
00105820 22865819-Fam1 PubMed: Maluenda 2016, Journal: Maluenda 2016 2-generation family, affected male/female fetuses, unaffected heterozygous carrier parents F;M no France - <0d - - - ? see paper; …, arthrogryposis multiplex congenita 2 2 Johan den Dunnen
00105821 22865819-Fam2 PubMed: Maluenda 2016, Journal: Maluenda 2016 2-generation family, affected fetus, unaffected heterozygous carrier parents M yes France - <0d - - - ? see paper; …, arthrogryposis multiplex congenita 1 1 Johan den Dunnen
00105822 22865819-Fam3 PubMed: Maluenda 2016, Journal: Maluenda 2016 2-generation family, affected male fetuses, unaffected heterozygous carrier parents M no France - <0d - - - ? see paper; …, arthrogryposis multiplex congenita 2 2 Johan den Dunnen
00105823 22865819-Fam4 PubMed: Maluenda 2016, Journal: Maluenda 2016 2-generation family, affected female fetus, unaffected heterozygous carrier parents F yes France - <0d - - - ? see paper; …, arthrogryposis multiplex congenita 1 1 Johan den Dunnen
00307179 D12-950 PubMed: Ravenscroft 2020, Journal: Ravenscroft 2020 family, 2 affected siblings - - Australia - - - - - FADS fetal akinesia sequence; decreased fetal movement; arthrogryposis; multiplex congenita hydrops fetalis; pterygium; hypoplastic heart; pulmonary hypoplasia; skeletal muscle hypertrophy; high palate 2 2 Gianina Ravenscroft
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