All individuals with variants in gene CHMP2B

19 entries on 1 page. Showing entries 1 - 19.
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00149250 - - - - - Denmark white - - - - FTD - 1 22 Marc Cruts
00149251 - - - - - - white - - - - FTD - 1 1 Marc Cruts
00149252 - - Mutation does not segregate with disease - - - - - - - - FTD - 1 1 Marc Cruts
00149253 - - - - - United Kingdom (Great Britain) white - - - - FTD - 1 1 Marc Cruts
00149254 - - - - - - - 71y - - - FTDALS - 1 1 Marc Cruts
00149255 - - - - - - - - - - - ? - 1 1 Marc Cruts
00149256 - - - - - Belgium white - - - - FTD - 1 1 Marc Cruts
00149257 - - - - - Belgium white 80y - - - ? - 1 1 Marc Cruts
00149650 - - - - - United Kingdom (Great Britain) white 55y - - - ALS17 - 1 1 Marc Cruts
00149679 - - - - - - - 70y - - - ALS17 - 1 1 Marc Cruts
00149680 - - - - - - - 52y - - - ALS17 - 1 1 Marc Cruts
00149681 - - - - - - - 74y - - - ALS17 - 1 1 Marc Cruts
00293476 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 57 Mohammed Faruq
00293477 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00293478 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 38 Mohammed Faruq
00304961 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00473290 Fam202268Pat527 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M no Iran - - - - - ALS onset 13-month ago; Abnormal gait, spastic; Muscle weakness & atrophy; Fasciculation; Spasticity; Hyperreflexia; Positive Gowers sign; Increased DTR; VEP test: electrical evidence of bilateral demyelination of the optic nerve; EMG-NCV: suggestive of UMN lesion. 1 1 Johan den Dunnen
00473310 Fam203028Pat548 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history F yes Iran - - - - - SMA onset 14y ago; Lower & upper distal muscle weakness & atrophy due to neuropathy; Difficulty heel & toe walking; EMG-NCV: chronic motor polyneuropathy/neuronopathy with addition evidence of bilateral CTS. 1 1 Johan den Dunnen
00473361 Fam206625Pat631 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M yes Iran - - - - - leukodystrophy Consanguineous parents ,sporadic case, onset 6y, lower and upper muscle weakness, foot drop , dysarthria, bulbar dysfunction, distal atrophy, gait abnormality, irritability and aggression, EDX normal report with central weakness impression , leuckodystrophy with thalamic involvement and mcp involvement reported in brain MRI 1 1 Johan den Dunnen
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