All individuals with variants in gene ZEB2

17 entries on 1 page. Showing entries 1 - 17.
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00000029 - PubMed: Almomani 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00037447 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00037448 - - - - - Germany - - - - - MEOAL;MMDS8 Mowat-Wilson syndrome 1 1 Andreas Laner
00037449 - - - - - Germany - - - - - ? CGH-array complex dysmorphy, kraniofaziale Dysmorphie, verstrichenes Philtrum, wide thumbs, Fingerpads, lange dichte Wimpern, Scapulae alatae, Enkopresis 1 1 Andreas Laner
00037450 - - - - - Germany - - - - - ? developmental delay 1 1 Andreas Laner
00081000 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - MOWS Mowat-Wilson syndrome (OMIM:235730) 1 1 Daniel Trujillano
00102081 P10 - - F no China - >08y - - - ID HP:0000252; HP:0001999; HP:0001250; HP:0007364; intellectual disability (HP:0001249) 1 1 Wenjuan Qiu
00133267 HK164C - - M - Hong Kong - - - - - HCAD - 1 1 Xuehan Zhuang
00150166 26539891-FamBAB3413 PubMed: Karaca 2015 - - - - - - - family structure in paper - ? intellectual diability, CCA, severe intellectual diability, epilepsy, no ambulation, pointed chin, cupped ears 1 1 Johan den Dunnen
00292250 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00316084 K107 PubMed: Heidet 2017 - - - France - - - - - CAKUT renal hypoplasia; preauricular pits 1 1 Johan den Dunnen
00319997 - - - F - - - - - - - ? Delayed speech and language development (HP:0000750); Seizure (HP:0001250); Global developmental delay (HP:0001263) 1 1 IMGAG
00374452 S-495 PubMed: Ganapathy 2019 - - - India - - - - - ? Craniosynostosis, macrocephaly, seizures, behavioural problems, delayed speech, hypermetropia, papilliedema and slender fingers 1 1 Johan den Dunnen
00374537 S-2908 PubMed: Ganapathy 2019 - - - India - - - - - ? Developmental delay, dolichocephaly, bilaterally raised ear lobule, broadening of eyelashes and undescended testis 1 1 Johan den Dunnen
00444047 PID_15 PubMed: Sarker 2023 no family history M - Bangladesh - - - - - DMD calf hypertrophy; Gower sign positive; elevated CPK; no feeding difficulties; no toe walking; poor walking/running ability; no difficulty climbing stairs; no waddling feet/gait; two seizures; muscle weakness; no skinny legs/arms; delayed developmental milestones; no intellectual disability; no delayed speech; not hyperactive 1 1 Johan den Dunnen
00449560 290575 - - F no Turkey - - - - - MOWS Neurodevelopmental delay, Ventricular septal defect, Patent ductus arteriosus, Complex febrile seizure, Microcephaly, Delayed speech and language development, Hypertelorism, Abnormality of the face, Delayed gross motor development 1 1 Andreas Laner
00453808 BAV249 PubMed: Mansoorshahi 2024 analysis 215 early-onset complications bicuspid aortic valve-affected families. - - United States - - - - - CHD - 1 1 Johan den Dunnen
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