All individuals with variants in gene WDR35

23 entries on 1 page. Showing entries 1 - 23.
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00108617 JWS_CED_2017_1 - - M no Poland Polish - - - - CED Craniosynostosis sagittal (HPO:000442), Craniosynostosis coronal (HPO:000440), Dolichocephaly (HPO: ), Nephronophthisis (HPO:000090), Sate 2 chronic kidney disease (HPO:0012624), short limbs (HPO:0009826), Narrow thorax (HPO:0000774), Brachydactyly (HPO:0001156), Abnormal teeth (HPO:0000164), Everted lower lip (HPO:0000233), Epicanthic folds (HPO:0000286) 2 1 Joanna Walczak-Sztulpa
00292530 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 268 Mohammed Faruq
00292531 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 10 Mohammed Faruq
00292532 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 17 Mohammed Faruq
00292533 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 179 Mohammed Faruq
00292534 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00300262 R03-342 PubMed: Duran 2017 fetus - - United States European - - - - SRTD 22w-delivery; scalp edema, low set ears; hypertelorism; thin upper lip and micrognathia; narrow and barrel shaped chest, short and bent ribs, handlebar clavicles; micromelia with bowing of the radii and ulnae; abnormal ilia with abnormal absent sciatic notch and unformed acetabular roof; micromelia; postaxial polydactyly in the hands and feet, and aphalangia in the hands 2 1 Johan den Dunnen
00300263 R10-483 PubMed: Duran 2017 - - - United States - - - - - SRTD 23w-delivery; scalp edema; very short, variably bent ribs, handlebar clavicles; micromelia with bowing of the radii and ulnae; flat acetabular roof, narrow sacrosciatic notch; micromelia, bending of the tibae and fibulae; poor mineralization of the hands and feet, no polydactyly 2 1 Johan den Dunnen
00304771 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 8 Mohammed Faruq
00304772 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00320364 - - - M - Poland - - - - - CED2 - 2 1 Joanna Walczak-Sztulpa
00320365 - - - M no Poland - 00y04m - - - CED2 - 2 1 Joanna Walczak-Sztulpa
00320367 - - - F no Poland - - - - - CED2 - 2 1 Joanna Walczak-Sztulpa
00320368 - - - F - Poland - - - - - CED2 - 2 1 Joanna Walczak-Sztulpa
00331593 13DG0792 , 13DG0793 PubMed: Maddirevula 2018 family, 2 affected (2F) F yes - Arab - - - - skeletal dysplasia Strabismus, Renal insufficiency, Hepatic fibrosis, Global developmental delay, Limb under No 1 2 LOVD
00387594 - PubMed: Yamamura 2019 Her father had A208P, and her mother had L712YfsTer20. novel p.A208P F no Japan Japanese - - - - retinal disease Intellectual disability, optic coloboma and cystic kidney 2 1 LOVD
00388409 R88-098A PubMed: Zhang-2019 - - - - white - - - - ? polydactyly 2 1 LOVD
00388410 R98-468C PubMed: Zhang-2019 - - - - white - - - - ? - 2 1 LOVD
00388411 R98-468D PubMed: Zhang-2019 - - - - white - - - - ? - 2 1 LOVD
00388455 R11-410A PubMed: Zhang-2019 Unsolved case: biallelic causative mutations not identify - - - South Asian - - - - ? polydactyly 1 1 LOVD
00388456 R10-471 PubMed: Zhang-2019 Unsolved case: biallelic causative mutations not identify - - - white - - - - ? polydactyly 1 1 LOVD
00393969 - PubMed: Strong-2020 - M - - - - - - - retinal disease ductal plate malformation, cirrhosis, developmental delay, hypertension, and abnormal kidney echogenicity 2 1 LOVD
00418506 Fam3 PubMed: He 2022 - - - China - - - - - ? - 1 1 Johan den Dunnen
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