All individuals with variants in gene PDSS1

10 entries on 1 page. Showing entries 1 - 10.
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00036493 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036494 - - - - - Germany - - - - - ? suspected mitochondrial disease, severe therapy-refractory epilepsy, severe hypotonia,mental retardation 1 1 Andreas Laner
00036495 - - - - - Germany - - - - - ? suspected mitochondrial disease, severe therapy-refractory epilepsy, severe hypotonia,mental retardation 1 1 Andreas Laner
00290031 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 48 Mohammed Faruq
00424939 Fam1 PubMed: Jurkute 2022 2-generation family, 1 affected, unaffected heterozygous carrier relatives F - United Kingdom (Great Britain) - - - - - RP hearing impairment, 48y-vision problems; 60y-nyctalopia; retinitis pigmentosa myopia, history left eye cystoid macular oedema, 55y-epiretinal membrane peeling; 8y-hearing impairmen, minor pericardial effusion (asymptomatic) 2 1 Johan den Dunnen
00424940 Fam2 PubMed: Jurkute 2022 2-generation family, 1 affected, unaffected parents F - United Kingdom (Great Britain) - - - - - RP decreased night vision, followed by peripheral visual field loss; retinitis pigmentosa, myopic astigmatism, left eye cystoid macular oedema; hearing impairment 2 1 Johan den Dunnen
00424941 Fam3 PubMed: Jurkute 2022 2-generation family, 1 affected, unaffected heterozygous carrier parents F - United Kingdom (Great Britain) - - - - - RP 30y-incidental finding during routine check-up, asymptomatic; 43y-lamellar hole, 52y- bilateral cataracts; mild hearing impairment (formally not investigated) 2 1 Johan den Dunnen
00424943 Fam4 PubMed: Jurkute 2022 2-generation family, 1 affected, unaffected parents M - United Kingdom (Great Britain) - - - - - RP 2y-hearing impairment, followed by vision problems; retinal dystrophy; 11y-unspecified chest pain, 15y-epistaxis, 17y-cardiac arrhythmia – bradycardia, 17y-syncope 1 1 Johan den Dunnen
00424947 Fam5 PubMed: Jurkute 2022 2-generation family, 1 affected, unaffected parents M - - - - - - - RP peripheral visual field loss; retinitis pigmentosa, myopic astigmatism, cataracts; hypertension, myocardial infarction 2 1 Johan den Dunnen
00424948 Fam6 PubMed: Jurkute 2022, 2-generation family, 1 affected, unaffected heterozygous carrier mother M - - - - - - - RP night blindness since childhood, 37y-glare sensitivity; retinitis pigmentosa, myopic astigmatism, right eye cataract ; premature birth, weight 1500 g, hemiplegia after birth disappeared within an hour; osteomalacia; 52y-myocardial infarction 2 1 Johan den Dunnen
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