All individuals with variants in gene ADSL

13 entries on 1 page. Showing entries 1 - 13.
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00150132 26539891-FamBAB5023 PubMed: Karaca 2015 - - - - - - - family structure in paper - ? intellectual diability, developmental delay 1 3 Johan den Dunnen
00180179 29286531-Pat31 PubMed: TumienÄ— 2018 - - - (Slovenia) - - - - - ? Epilepsy (HP:0001250), generalized myoclonic seizures (HP:0002123), developmental regression (HP:0002376), severe global developmental delay (HP:0011344), epicanthus (HP:0000286). 2 1 Johan den Dunnen
00218092 128850 - sister (MGZ# 128851) also affected M ? Germany - - - - - DD Profound global developmental delay (HP:0012736), Poor speech (HP:0002465), Abnormality of facial skeleton (HP:0011821), Growth abnormality (HP:0001507), biochemical Adenylosuccinase deficiency 2 1 Andreas Laner
00293127 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00293128 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00293129 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00293131 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00374180 S-5239 PubMed: Ganapathy 2019 - - - India - - - - - ? Motor delay, hypotonia, recurrent chesty episode, severe motor axonal neuropathy, weakness in left leg, central hypothyroidism and seizures 1 1 Johan den Dunnen
00374646 S-1710 PubMed: Ganapathy 2019 - - - India - - - - - ? - 1 1 Johan den Dunnen
00375654 Pat48 PubMed: Srivastava 2014 - - - United States - - - - - ? intellectual disability/developmental delay; ophthalmoplegia, strabismus; hypotonia, broad-based gait; MRI brain ventriculomegaly, ventricular asymmetry 2 1 Johan den Dunnen
00379542 183667 - - F no Germany - - - - - ADLSD Psychomotor delay, severe, Visual impairment, Seizure, Global developmental delay, Hypotonia, 2 1 Andreas Laner
00387794 M8600562 PubMed: Hu 2019 family, 3 affected individuals, second cousin parents - yes Iran Persia - - - - ID syndromic intellectual disability, no microcephaly, epilepsy, autism 1 3 Johan den Dunnen
00431871 SIDS038 - - M - Switzerland Europe 00y04m - - - SIDS SIDs 1 1 Cordula Haas
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