All individuals with variants in gene SLC25A19

14 entries on 1 page. Showing entries 1 - 14.
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00207883 28771251-Pat11 PubMed: Lionel 2018 - F - Canada - - - - - ? Global developmental delay; episodic metabolic acidosis; abnormal thalamic MRI signal intensity 2 1 Johan den Dunnen
00208793 - - - F - Germany - - - - - - HP:0011805 (Abnormality of muscle morphology); HP:0003198 (Myopathy) 1 1 Andreas Laner
00213102 12185364-Fams PubMed: Rosenberg 2002 23 nuclear families connected to a single ancestral couple, 16 affected F;M yes United States Amish - - - - MCPHA see paper; ... 1 16 Johan den Dunnen
00213103 19798730-Fam PubMed: Spiegel 2009 4-generation family, 4 affected (3F, M), unaffected heterozygous carrier parents F;M yes Israel Arab, muslim - - - - THMD see paper; ... 1 4 Johan den Dunnen
00213107 28856750-Pat75 PubMed: Ortigoza-Escobar 2017 - F yes Germany white - - - - THMD see paper; ... 1 1 Johan den Dunnen
00226659 P71 PubMed: Ortigoza-Escobar 2017 2-generation family, 42 affected, unaffected heterozygous carrier parents - yes Israel Arab - - - - THMD encephalopathy, hypotonia, dysphagia, dysarthria; neuroimaging abnormalities: caudate, putamen; outcome: peripheral neuropathy, ADHD 1 4 Johan den Dunnen
00226660 P72 PubMed: Ortigoza-Escobar 2017 P72 - yes Israel Arab - - - - THMD encephalopathy, hypotonia; neuroimaging abnormalities: caudate, putamen; outcome: peripheral neuropathy, ADHD 1 1 Johan den Dunnen
00226661 P73 PubMed: Ortigoza-Escobar 2017 P73 - yes Israel Arab - - - - THMD encephalopathy, hypotonia, status dystonicus, dysphagia, dysarthria; neuroimaging abnormalities: caudate, putamen; outcome: peripheral neuropathy, movement disorder 1 1 Johan den Dunnen
00226662 P74 PubMed: Ortigoza-Escobar 2017 P74 - yes Israel Arab - - - - THMD encephalopathy, hypotonia, status dystonicus, dysphagia, dysarthria; neuroimaging abnormalities: caudate, putamen, thalamus; outcome: peripheral neuropathy, movement disorder 1 1 Johan den Dunnen
00226663 P75 PubMed: Ortigoza-Escobar 2017 - - yes Germany white, European - - - - THMD encephalopathy, tremor, dystonia, opistothonus, vertigo, ataxia, dysphagia; neuroimaging abnormalities: caudate, putamen, globus pallidus, corticosubcortical 1 1 Johan den Dunnen
00291842 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00361609 12DG1007 PubMed: Anazi 2017 familial - yes Saudi Arabia - - - - - ID not syndromic; intellectual disability, Microcephaly 1 1 Johan den Dunnen
00374856 S-5807 PubMed: Ganapathy 2019 - - - India - - - - - ? - 1 1 Johan den Dunnen
00458019 FamPat13(II2) PubMed: Peng 2017 2-generation family, 2 affected brothers, unaffected parents M - - Hispanic - - - - ? see paper; ..., no microcephaly; optic atrophy; MRI brain normal; no seizures; EEG normal; global development delay; regression; hypotonia; spasticity 1 2 Johan den Dunnen
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