All individuals with variants in gene ARSG

18 entries on 1 page. Showing entries 1 - 18.
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00249645 - - healhty carrier dogs - no - - - - - - Healthy/Control - 1 91 Sara Mole
00249646 - - - - no - - - - - - CLN late onset 1 138 Sara Mole
00308952 - PubMed: Sharon 2019 1 IRD families - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00309516 MOL0120 PubMed: Khateb 2018 4-generation family, 2 affected brothers M yes Israel Yemenite;Jewish - - - - retinal disease see paper; ... 1 2 Johan den Dunnen
00309517 MOL0737 PubMed: Khateb 2018 3-generation family, 2 affected sisters F - Israel Yemenite;Jewish - - - - retinal disease see paper; ... 1 2 Johan den Dunnen
00309518 TB55 PubMed: Khateb 2018 3-generation family, 1 affected F - Israel Yemenite;Jewish - - - - retinal disease see paper; ... 1 1 Johan den Dunnen
00410956 - PubMed: Abad Morales 2020 - F yes - Spanish - - - - retinal disease pericentral retinal pigment epithelium alteration that extended beyond the optic nerve, with midperipheral bone spicule-like disturbances; see paper 1 1 LOVD
00410957 Individual 1 PubMed: Peter 2021 - F ? Portugal Portuguese - - - - retinal disease nyctalopia, peripheral visual field loss, photopsia, and dyschromatopsia for dark tones. See paperÂ… 1 1 LOVD
00410958 Individual 2 PubMed: Peter 2021 - F ? Portugal Portuguese - - - - retinal disease VA: greatly diminished (only detect hand movements (both eyes)). Round cortical lens opacities were observed bilaterally. Pale optic discs and vascular attenuation were observed. See paperÂ… 2 1 LOVD
00410959 - PubMed: Fowler 2021 - M ? (United States) Persian - - - - retinal disease previously diagnosed with macular edema; 20 years of progressive SNHL, and 10 years of progressive peripheral vision loss and pigmentary retinopathy. Late-onset sensorineural hearing loss without vestibular abnormalities and a late-onset retinal involvement that on DFE that showed the ring-shaped retinal atrophy encompassing the vascular arcades temporally and extending nasal to optic nerve with preservation of the mid- and far-periphery. See paper... 1 1 LOVD
00412481 D.II-2 PubMed: Delvallee 2021 - - - France - - - - - retinal disease sensorineural features: retinal dystrophy; abnormalities of the hands and feet: postaxial polydactyly: hands; clinodactyly; obesity: BMI (29.3); slow ideation; urogenital anomalies; other clinical features: hepatic steatosis, lumbar stenosis, iron deficiency 1 1 LOVD
00430927 PatD;071951 PubMed: Velde 2022, Journal: Velde 2022, PubMed: de Bruijn 2023 - M - Ireland white - - - - retinal disease see paper 2 1 Janine Reurink
00430939 PatF PubMed: Velde 2022, Journal: Velde 2022 - F - Germany - - - - - retinal disease see paper 2 1 Janine Reurink
00430986 PatN PubMed: Velde 2022, Journal: Velde 2022 - M - Netherlands Turkey - - - - retinal disease see paper; ..., 46y-peripheral vision loss, night blindness 2 1 Johan den Dunnen
00430999 ARSG-1 PubMed: Igelman 2021 - M no - - - - - - retinal disease see paper; ..., cataract; no macular findings; no sensorineural hearing loss; no vestibular symptoms 2 1 Johan den Dunnen
00431000 ARSG-2 PubMed: Igelman 2021 - F no - - - - - - retinal disease see paper; ..., no cataract; foveal sparing atrophy; ffERG moderate rod-cone dystrophy; 50y-moderate sensorineural hearing loss, unclear progression; no vestibular symptoms 2 1 Johan den Dunnen
00431001 ARSG-29692 PubMed: Igelman 2021 - F yes - - - - - - retinal disease see paper; ..., cataract; atrophy; 50y-severe sensorineural hearing loss, stable; vestibular symptoms 1 1 Johan den Dunnen
00447445 USHII-369 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - ? - 1 1 Johan den Dunnen
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