All individuals with variants in gene MT-TL1

16 entries on 1 page. Showing entries 1 - 16.
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00180181 29286531-Pat33 PubMed: TumienÄ— 2018 - - - (Slovenia) - - - - - ? Epilepsy (HP:0001250), generalized myoclonic seizures (HP:0002123), sensorineural hearing impairment (HP:0000407), glucose-intolerance (HP:0001952), stroke-like episodes (HP:0002401). 1 1 Johan den Dunnen
00308521 - PubMed: Holtan 2020 1 patient with variant in heterozygous or compound heterozygous form - - Norway - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00328346 - de Boer 2021, submitted - M ? Netherlands - - - - - mitochondrial Severe intellectual disability, brain imaging abnormalities (pachygyria, polymicrogyria, white matter abnormalities, in retrospect signs of stroke on brain CT), spastic tetraparesis, oral dystonia and dystonia of hands and feet, epilepsy, episodic headaches with nausea and emesis, adverse drug reactions, feeding difficulties, secondary microcephaly in childhood, low body weight, drooling, severe progressive neuromuscular scoliosis and congenital hip dysplasia, dental and gingival abnormalities, facial dysmorphisms 1 1 Elke de Boer
00332052 Pat190 PubMed: Birtel 2018 patient M - Germany - - - - - retinal disease incidental finding; scotopic ERG not analyzable; photopic ERG not analyzable 1 1 LOVD
00332053 Pat191 PubMed: Birtel 2018 patient F - Germany - - - - - retinal disease reduced visual acuity; scotopic ERG normalreduced; photopic ERG borderline 1 1 LOVD
00389404 688 PubMed: Weisschuh 2020 Filing key number: 249, unclassified / mixed, no patient Ids, consecutive numbers given F - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00389405 689 PubMed: Weisschuh 2020 Filing key number: 249, unclassified / mixed, no patient Ids, consecutive numbers given F - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00391177 139 PubMed: Gliem 2020 - M - (Germany) - - - - - retinal disease - 1 1 LOVD
00430375 patient PubMed: Giannese 2023 - F - Italy - - - - - ? see paper; ..., encephalomyopathy, chronic proteinuric kidney disease; adulthood migraine; 38y-progressive sensorineural hearing loss, fatigue, bilateral cataracts, pigmented retinopathy; muscle biopsy myopathic changes, scattered ragged red/blue fibers, COX negative fibers 1 1 Johan den Dunnen
00435658 HN- F163-II-1 - - M no Germany - - - - - MELAS HP:0010305, HP:0002023, HP:0004871, HP:0002032, HP:0002750, HP:0006482 1 1 Jasmina Comic
00450883 071451 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - F - - - - - - - macular dystrophy - 1 1 Rebekkah Hitti-Malin
00450884 071508 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - M - - - - - - - macular dystrophy - 1 1 Rebekkah Hitti-Malin
00450885 071801 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - F - - - - - - - macular dystrophy - 1 1 Rebekkah Hitti-Malin
00450886 072060 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - F - - - - - - - macular dystrophy - 1 1 Rebekkah Hitti-Malin
00450887 072855 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - F - - - - - - - macular dystrophy - 1 1 Rebekkah Hitti-Malin
00450888 DNA18-14353B PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - F - - - - - - - macular dystrophy - 1 1 Rebekkah Hitti-Malin
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