All individuals with variants in gene SLC25A24

11 entries on 1 page. Showing entries 1 - 11.
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AscendingIndividual ID     

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VIP     

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00147047 29100094-Pat1 PubMed: Writzl 2017 2-generation family, 1 affected, unaffected non-carrier parents M - Slovenia - - - - - ? early aging, bone dysplasia, characteristic face, early demise 1 1 Johan den Dunnen
00147048 29100094-Pat2 PubMed: Writzl 2017 2-generation family, 1 affected, unaffected non-carrier parents M - France - - - - - ? early aging, bone dysplasia, characteristic face, early demise 1 1 Johan den Dunnen
00147049 29100094-Pat3 PubMed: Writzl 2017 2-generation family, 1 affected, unaffected non-carrier parents F - Spain - - - - - ? early aging, bone dysplasia, characteristic face, early demise 1 1 Johan den Dunnen
00147050 29100094-Pat4 PubMed: Writzl 2017 2-generation family, 1 affected, unaffected non-carrier parents F - Italy - - - - - ? early aging, bone dysplasia, characteristic face, early demise 1 1 Johan den Dunnen
00147051 29100093-Pat1 PubMed: Ehmke 2017 2-generation family, 1 affected, unaffected non-carrier parents F - Poland - - - - - ? hypertrichosis, progeroid appearance, mitochondrial dysfunction 1 1 Johan den Dunnen
00147052 29100093-Pat2 PubMed: Ehmke 2017 2-generation family, 1 affected, unaffected non-carrier parents F - Hungary - - - - - ? hypertrichosis, progeroid appearance, mitochondrial dysfunction 1 1 Johan den Dunnen
00147053 29100093-Pat3 PubMed: Ehmke 2017 2-generation family, 1 affected, unaffected non-carrier parents F - Germany - - - - - ? hypertrichosis, progeroid appearance, mitochondrial dysfunction 1 1 Johan den Dunnen
00147054 29100093-Pat4 PubMed: Ehmke 2017 2-generation family, 1 affected, unaffected non-carrier parents F - Turkey - - - - - ? hypertrichosis, progeroid appearance, mitochondrial dysfunction 1 1 Johan den Dunnen
00147055 29100093-Pat5 PubMed: Ehmke 2017 2-generation family, 1 affected, unaffected non-carrier parents F - - Europe, north - - - - ? hypertrichosis, progeroid appearance, mitochondrial dysfunction 1 1 Johan den Dunnen
00227835 - - 4-generation family, 7 affecteds, unaffected heterozygous family members M yes Palestine - >26y - - - DFNB severe/profound hearing loss; no hearing aid; no motor delay; no communicative delay; no cognitive impairment; no ventriculomegaly; corpus callosum short and thin; heterotopia moderate; frontal polymicrogyria moderate; cerebellar dysplasia; moderate interhemispheric cyst 1 7 LOVD
00374120 - PubMed: Lefebvre 2021 fetus F - France - - - - - ? 20w-fetus, ultrasound small for gestational age, cardiopathy, syndactyly; autopsy intrauterine growth retardation, hydramnios, microcrania, retrognathia, vermian hypoplasia, auricular external canal atresia, broad hands, syndactyly, interauricular communication 1 1 Johan den Dunnen
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