All individuals with variants in gene DNAH7

17 entries on 1 page. Showing entries 1 - 17.
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00050341 - PubMed: DDDS 2015, Journal: DDDS 2015 proband - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 2 1 Johan den Dunnen
00103894 28327206-PatBH6695_1 PubMed: Eldomery 2017, Journal: Eldomery 2017 - - - United States - - - - - ? dysmorphic feat, seizures, thin corpus callosum, basal ganglia changes, hyper, hypotonia, respiratory difficulty 1 1 Johan den Dunnen
00265203 Pat PubMed: Kiselev 2019 - F - Sweden - - - - - MD see paper; ..., cardiomyopathy, limb-girdle type muscular dystrophy 1 1 Johan den Dunnen
00265670 - - - M no Russian Federation - - - - - ? - 1 1 Victoria Serzhanova
00292523 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 35 Mohammed Faruq
00292524 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 71 Mohammed Faruq
00292525 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 64 Mohammed Faruq
00292526 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 90 Mohammed Faruq
00292527 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 14 Mohammed Faruq
00304768 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00304769 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00304770 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00327461 M68 II-1 Doucette 2021, submitted Only Affected brother of a 4 member family. 1 unaffected sister and unaffected parents. Patient has an occult macular dystrophy though no RP1L1 variants were noted. M - Canada - - - Yes - maculopathy Fundus: No specific findings OCT: Normal ERG:Central loss on multi-focal electroretinogram (abnormal ERG HP:0000512) - Reduced Visual Acuity 20/40 OU (HP:0007663) 2 1 Lance P Doucette
00402308 NK-0305 - - M yes China Han Chinese - - - WES INFM - 1 1 Yang Gao
00443877 FamDPatV2 PubMed: Chatron 2020 4-generation family, affected brother/sister, unaffected heterozygous parents/relatives M yes Iran - - - - - DEE see paper; ..., 1d-myoclonic seizure; 10y-last seizure; EEG at onset dysrhythmia; 10y-last seizure; axial hypotonia, spasticity, dystonia; profound intellectual disability; no pes equinovarus; no omphalocele; no cleft palate; no joint contractures; no dysmorphic facial features; MRI brain normal 1 2 Johan den Dunnen
00443878 FamDPatV3 PubMed: Chatron 2020 sister F yes Iran - - - - - DEE see paper; ..., 7d-epileptic spasms, myoclonic seizure; no seizures reported for 2 m; EEG at onset suppression-burst pattern/burst attenuation; axial hypotonia, mild dystonia; profound intellectual disability; no pes equinovarus; no omphalocele; no cleft palate; no joint contractures; no dysmorphic facial features; MRI brain posterior cervical junction notch 1 1 Johan den Dunnen
00462300 051-039-KUY PubMed: Boissel 2017 analysis 101 stillborn fetuses with severe prenatal anoalies - - Canada - 0d - - - ? 20gw-triventriculomegaly, occipital encephalocele 2 1 Johan den Dunnen
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