All individuals with variants in gene CDH3

33 entries on 1 page. Showing entries 1 - 33.
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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) 2 1 Yu Sun
00155402 MOL1145 PubMed: Beryozkin 2015, PubMed: Sharon 2019 - M no Israel Druze - - - - retinal disease - 1 3 Dror Sharon
00296031 patient PubMed: Blanco-Kelly 2017 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Spain - - - - - ? see paper; initial diagnosis keratosis follicularis spinulosa decalvans and retinitis pigmentosa inversa; 1y-absence growing hair, pale skin, sparse scalp hair, punctiform follicular keratosis on cheeks, forehead, eyebrows and anterior surface arms and posterior surface legs, erythema with follicular hyperkeratosis and reduction hair density eyebrows; skin biopsy reduction number scalp follicles, absence seborrheic glands, infundibular cyst with keratin granules; 2y-retinal alteration, ... 2 1 Johan den Dunnen
00309017 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00309018 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00309019 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00309020 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00328248 G008993 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - retinal disease - 1 1 LOVD
00331349 14DG0186 , 14DG0187 PubMed: Maddirevula 2018 family M yes - Arab - - - - skeletal dysplasia Ectrodactyly, Macular dystrophy 1 1 LOVD
00331350 12DG1777, 12DG2033 PubMed: Maddirevula 2018 family M yes - Arab - - - - skeletal dysplasia Rod-cone dystrophy, Abnormal facial shape, Ectrodactyly 1 1 LOVD
00331979 Pat116 PubMed: Birtel 2018 patient M - Germany - - - - - retinal disease reduced visual acuity; scotopic ERG normal; photopic ERG borderline 1 1 LOVD
00335095 8326 PubMed: Haer-Wigman 2017 patient - no Netherlands - - - - - ? 2y-diagnosis visual impairment 2 1 LOVD
00382510 372 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - retinal disease - 1 1 LOVD
00383412 - PubMed: Khan 2019 - M - - - - - - - retinal disease - 1 1 LOVD
00384031 RP-1777 PubMed: Martin Merida 2019 - ? - Spain - - - - - retinal disease - 2 1 LOVD
00385107 IV:3 PubMed: Schauren 2020 Family #1 F - Brazil - - - - - retinal disease - 1 1 LOVD
00385108 IV:4 PubMed: Schauren 2020 Family #1 M - Brazil - - - - - retinal disease - 1 1 LOVD
00385109 IV:5 PubMed: Schauren 2020 Family #1 F - Brazil - - - - - retinal disease - 1 1 LOVD
00385110 IV:6 PubMed: Schauren 2020 Family #1 M - Brazil - - - - - retinal disease - 1 1 LOVD
00385111 III:1 PubMed: Schauren 2020 Family #2 F - Brazil - - - - - retinal disease - 2 1 LOVD
00385112 III:2 PubMed: Schauren 2020 Family #2 F - Brazil - - - - - retinal disease - 2 1 LOVD
00385113 III:10 PubMed: Schauren 2020 Family #3 M - Brazil - - - - - retinal disease - 1 1 LOVD
00385114 III:11 PubMed: Schauren 2020 Family #3 M - Brazil - - - - - retinal disease - 1 1 LOVD
00386223 RPN-379 PubMed: Rodriguez-Munoz 2020 family fRPN-179, proband F - Spain - - - - - retinal disease - 1 1 LOVD
00386280 RPN-188 PubMed: Rodriguez-Munoz 2020 family fRPN-71, proband F - Spain - - - - - retinal disease - 1 1 LOVD
00386287 RPN-461 PubMed: Rodriguez-Munoz 2020 family fRPN-AP, proband F - Spain - - - - - retinal disease - 1 1 LOVD
00388495 14021329 PubMed: Ellingsford 2018 - - - United Kingdom (Great Britain) - - - - - retinal disease - 1 1 LOVD
00389501 785 PubMed: Weisschuh 2020 Filing key number: 305, Stargardt Disease, no patient Ids, consecutive numbers given M - Germany - - - - - retinal disease age at genetic diagnosis mentioned 2 1 LOVD
00390199 G008993 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - - - - - - - retinal disease - 1 1 LOVD
00393332 RP-050 PubMed: Ng 2021 - F ? China - - - - - retinal disease - 1 1 LOVD
00393333 RP-053 PubMed: Ng 2021 - M ? China - - - - - retinal disease - 1 1 LOVD
00393334 RP-113 PubMed: Ng 2021 - F ? China - - - - - retinal disease - 1 1 LOVD
00450733 070565 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - F - - - - - - - macular dystrophy - 2 1 Rebekkah Hitti-Malin
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