All individuals with variants in gene EBP

39 entries on 1 page. Showing entries 1 - 39.
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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) 4 1 Yu Sun
00155194 3(III4) personal communication 3-generation family, 2 affected cousins, cousin of 4(III8) M - - - - - - - ? TSH-XL, hypogonadism (HP:0000135), mild hypocortisolism (HP:0008163) 1 2 Jacopo Celli
00155195 4(III8) personal communication Cousin of 3(III4) M - - - - - - - ? TSH-XL, hypogonadism (HP:0000135), mild hypocortisolism (HP:0008163) 1 1 Jacopo Celli
00155196 - - diagnosis in utero F no France - - - - - CPDX2 severe foetal form 1 1 Fabienne Dufernez
00155197 - - diagnosis in utero F no France - - - - - CPDX2 severe foetal form 1 1 Fabienne Dufernez
00155198 - - diagnosis in utero F no France - - - - - CPDX2 severe foetal form 1 1 Fabienne Dufernez
00155199 - - father germinal mosaicism, 2 foetus abortion, diagnosis in utero F no France - - - - - CPDX2 severe foetal form 1 1 Fabienne Dufernez
00163788 - - - F no France - 00y09m - - - CPDX2 typical skeletal features, ochtyosis and patchy alopecia 1 1 Fabienne Dufernez
00163789 - - - F no France - 00y09m - - - CPDX2 typical skeletal features, ichtyosis and patchy alopecia 1 1 Fabienne Dufernez
00163790 - - - F no France - 21y - - - CPDX2 typical skeletal features, ichtyosis and patchy alopecia 1 1 Fabienne Dufernez
00163791 - - - F no France - 00y01m - - - CPDX2 typical skeletal features, ichtyosis and patchy alopecia 1 1 Fabienne Dufernez
00163792 - - - F no France - 00y01m - - - CPDX2 several fetal form 1 1 Fabienne Dufernez
00163793 - - - - no France - 17y - - - CPDX2 typical skeletal features, ichtyosis and patchy alopecia 2 1 Fabienne Dufernez
00163794 - - diagnosis in utero F no France - 00y00m00d - - - CPDX2 diagnosis in utero 1 1 Fabienne Dufernez
00163795 - - dead 2y F no France - - - - - CPDX2 severe fetal form 1 1 Fabienne Dufernez
00163796 - - diagnosis in utero F no France - - - - - CPDX2 severe fetal form 1 1 Fabienne Dufernez
00163797 - - - F no France - 00y00m01d - - - CPDX2 typical skeletal features, ichtyosis and patchy alopecia 1 1 Fabienne Dufernez
00163798 - - - F no France - 20y - - - CPDX2 typical skeletal features, ichtyosis and patchy alopecia 1 1 Fabienne Dufernez
00163799 - - diagnosis in utero, 38 year-old mother F no France - - - - - CPDX2 severe fetal form 1 1 Fabienne Dufernez
00163800 - - - F no France - 04y - - - CPDX2 phenotype limited to skin, ichtyosis without skeletal features 1 1 Fabienne Dufernez
00163801 - - diagnosis in utero M no France - - - - - CPDX2 severe fetal form 1 1 Fabienne Dufernez
00163802 - - - F no France - 15y - - - CPDX2 phenotype limited to skin, ichtyosis without letal features 1 1 Fabienne Dufernez
00163803 - - - F no France - 12y - - - CPDX2 typical skeletal features, ichtyosis and patchy alopecia 1 1 Fabienne Dufernez
00163804 - - - F no France - 02y - - - CPDX2 phenoype limited to skin, ichtyosis without skeletal features 1 1 Fabienne Dufernez
00163805 - - - F no France - 00y01m - - - CPDX2 phenotype limited to skin, ichtyosis without skeletal features 1 1 Fabienne Dufernez
00163806 - - - F no France - 00y01m - - - CPDX2 typical skeletal features, ichtyosis and patchy alopecia 1 1 Fabienne Dufernez
00163807 - - diagnosis in utero F no France - - - - - CPDX2 severe fetal form 1 1 Fabienne Dufernez
00163808 - - - F no France - 21y - - - CPDX2 phenotype limited to skin, ichtyosis without skeletal features 1 1 Fabienne Dufernez
00163809 - - - F no France - - - - - CPDX2 typical skeletal features, ichtyosis and patchy alopecia 1 1 Fabienne Dufernez
00163810 - - diagnosis in utero - no France - - - - - CPDX2 phenotype limited to skin, ichtyosis without skeletal features 1 1 Fabienne Dufernez
00163811 - - diagnosis in utero F no France - - - - - CPDX2 severe fetal form 1 1 Fabienne Dufernez
00163812 - - diagnosis in utero F no France - - - - - CPDX2 severe fetal form 1 1 Fabienne Dufernez
00163813 - - - F no France - 10y - - - CPDX2 phenotype limited to skin, ichtyosis without skeletal features 1 1 Fabienne Dufernez
00234006 case report PubMed: Patrizi 2012 - F - Italy white - - - - FDH basal cell carcinomas; skin hypoplasia (HP:0008065), hyperpigmentation skin (HP:0000953), fat herniation (HP:0008441), no papilloma periorally (-HP:0040167), papilloma elsewhere (HP:0012740); syndactyly (HP:0001159), no scoliosis (-HP:0002650), no polydactyly (-HP:0010442), assymmetrical skeletal defects (HP:0011842), no ectrodactyly (-HP:0100257), oligodactyly (HP:0012165); , no cleft lip/palate (-HP:0000202); no microphthalmia (-HP:0000568), ; osteopathia striata (HP:001074), no mammary hypoplasia in adults (-HP:0003187), height not less than P3-P10 (-HP:0004322), 1 2 Maria Paola Lombardi
00295069 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 12 Mohammed Faruq
00295070 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 9 Mohammed Faruq
00295449 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00445041 CPXD00571 PubMed: Kessel 2021 family, 2 affected - - Denmark - - - - - CTRCT bilateral cataract, chondrodysplasia punctata 1 2 Johan den Dunnen
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