All individuals with variants in gene ERCC8

22 entries on 1 page. Showing entries 1 - 22.
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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) 2 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) 3 1 Yu Sun
00057256 - PubMed: Rump 2016 - M yes - - - - - - CSA Microcephaly HP:0000252 1 1 Birgit Sikkema-Raddatz
00230985 - PubMed: Laugel et al (2010) - - - - - - - - - CS - 1 1 SIB - Livia Famiglietti
00230986 - PubMed: Ridley et al (2005) - - - - - - - - - CS - 1 1 SIB - Livia Famiglietti
00230987 - PubMed: Laugel et al (2010) - - - - - - - - - CS - 1 1 SIB - Livia Famiglietti
00230988 - PubMed: Laugel et al (2010) - - - - - - - - - CS - 1 1 SIB - Livia Famiglietti
00230989 - PubMed: Cao et al (2004) - - - - - - - - - CS - 1 1 SIB - Livia Famiglietti
00230990 - PubMed: Laugel et al (2010) - - - - - - - - - CS - 1 1 SIB - Livia Famiglietti
00230991 - PubMed: Nardo et al (2009) - - - - - - - - - UVSS - 1 1 SIB - Livia Famiglietti
00293887 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 14 Mohammed Faruq
00295656 - - - M - - - - - - - ? Spasticity (HP:0001257); Global developmental delay (HP:0001263); Microcephaly (HP:0000252) 1 1 Andreas Laner
00307944 17DG0767 PubMed: Anazi 2017 familial M - - - - - - - ID see paper; ..., Global developmental delay, Microcephaly, Severe photosensitivity, Congenital cataract 1 1 Johan den Dunnen
00373719 iw110 - - M no China Chinese - - - - CSA HP:0001276; HP:0001249; HP:0006817; HP:0000238; HP:0100702; HP:0001263; HP:0000750; HP:0001181; HP:0002194; HP:0010862; HP:0001883 2 1 Wenjuan Qiu
00374314 S-3631 PubMed: Ganapathy 2019 - - - India - - - - - ? Cerebral atrophy and pigmentation changes in the retinal fundus 2 1 Johan den Dunnen
00416849 16 PubMed: Rump 2016 - M - - - - - - - CSA brain magnetic resonance imaging: leucodystrophy, cerebral and cerebellar atrophy; additional clinical featuresshort stature, truncal hypotonia, spasticity, contractures, scoliosis, deafness, pigmentary retinopathy, mildly enlarged liver and elevated aminotransferase, feeding problems, cryptorchid testis, severe developmental delay, progressive disease course (consanguineous parents) 1 1 LOVD
00433353 Pat3;Pat22 PubMed: Duerinckx 2020, PubMed: Duerinckx 2021 patient F yes Turkey - - - - - microcephaly Cockayne syndrome; birth OFC (SD-1), weigth (SD-0.5), length (SD-0.5); OFC (SD-6), weigth (SD-3), length (SD-6); 22m-generalized, tonic‐clonic, treatment VPA; severe intellectual disability; birth OFC (SD-1), weigth (SD-0.5), length (SD-0.5); OFC (SD-6), weigth (SD-3), length (SD-6); 22m-generalized, tonic‐clonic, treatment VPA; severe intellectual disability 1 1 Johan den Dunnen
00465605 - - - - - - - - - - - CSA - 1 1 Min Peng
00465606 - - - - - - - - - - - CSA - 1 1 Min Peng
00465607 - - - - - - - - - - - CSA - 2 1 Min Peng
00466859 NDSF02-1 - 2-generation family, 2 affected (F, M), unaffected heterozygous carrier parents F - Pakistan South asian - - - - CS - 1 2 Arisha Rasheed
00466860 NDSF02-2 - sib M yes Pakistan South asian - - - - CS - 1 1 Arisha Rasheed
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