All individuals with variants in gene KCTD7

12 entries on 1 page. Showing entries 1 - 12.
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Owner     
00050418 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? seizures, developmental regression, abnormality of the skull, abnormal facial shape, cerebral atrophy 2 1 Johan den Dunnen
00240407 example 2 PubMed: Fresard 2019 2-generation family, affected sister/brother F;M - Canada Hispanic - - - - DD developmental regression after typical development until 18m, manifesting with loss of milestones including head control and speech; 21m-tremors; 22m-seizures; occasional myoclonus; brother 5y onset 13m ataxia, autism, developmental delay, recurrent febrile seizures, absent speech 1 2 Johan den Dunnen
00294490 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 67 Mohammed Faruq
00303010 Pat55 PubMed: Helbig 2016 - - - United States - - - - - seizures Progressive Myoclonus Epilepsy; age onset childhood 2 1 Johan den Dunnen
00307873 ? - - F yes Saudi Arabia - - - - - EPM3;CLN14 Global developmental delay, Seizures, Abnormal facial shape 1 1 Corina-Marcela Rus
00361591 13DG1863 PubMed: Anazi 2017 familial M yes Saudi Arabia - - - - - ID not syndromic; Neurodegeneration 1 1 Johan den Dunnen
00361905 - - - - - - - - - - - EPM3;CLN14, FMFD Neuroregression, myoclonic epilepsy 1 1 Anju Shukla
00374637 S-5954 PubMed: Ganapathy 2019 - - - India - - - - - ? - 1 1 Johan den Dunnen
00374676 S-2377 PubMed: Ganapathy 2019 - - - India - - - - - ? - 1 1 Johan den Dunnen
00387819 M8700126 PubMed: Hu 2019 family, 3 affected individuals, first cousin parents - yes Iran Persia - - - - ID syndromic intellectual disability, no microcephaly, epilepsy 1 3 Johan den Dunnen
00388289 4 PubMed: Kozina 2020 - M no Russia - - - - - CLN Cognitive and motor deterioration, ataxia, epileptic paroxysms, and MRI signs of cerebellar subatrophy 2 1 LOVD
00448514 284164 - - F yes Saudi Arabia - - - - - EPM3;CLN14 Global developmental delay, Intellectual disability, Cerebral palsy, Seizure, Myoclonic seizures, Delayed speech and language development 1 1 Andreas Laner
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