All individuals with variants in gene AHDC1

21 entries on 1 page. Showing entries 1 - 21.
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00016586 - PubMed: Xia 2014 2-generation family, 1 affected F no (United States) European - - - - ? 18m-no words, no sitting, hypotonia, failure to thrive, low-set ears, esotropia, upslanting palpebral fissures, micrognathia, flat nasal bridge, laryngomalacia, obstructive sleep apnea 1 1 Marianne Vos (LOVD-team)
00016587 - PubMed: Xia 2014 2-generation family, 1 affected F ? (United States) South Asian - - - - ? 4y-two words; 19m-sitting; 24m-walking; hypotonia, failure to thrive, protuberant ears, upslanting palpebral fissures, flat nasal bridge, obstructive sleep apnea 1 1 Marianne Vos (LOVD-team)
00016588 - PubMed: Xia 2014 2-generation family, 1 affected M ? (United States) European - - - - ? mild intellectual disability; 1y-first words; persistent speech therapy; 9m-sitting; 18m-walking; hypotonia, failure to thrive, protuberant low-set ears, small earlobes, hypertelorism, downslanting palpebral fissures, mild ptosis, micrognathia, laryngomalacia, obstructive sleep apnea 1 1 Marianne Vos (LOVD-team)
00016589 - PubMed: Xia 2014 2-generation family, 1 affected M ? (United States) European - - - - ? intellectual disability, (moderate to severe), no words, noncommunicating autism; 15m-sitting; no independent ambulation, hypotonia, failure to thrive, upturned earlobes, hypertelorism, esotropia, flat nasal bridge, suspected tracheomalacia in infancy, history of snoring; no macrodontia, no skeletal defects, nor other features of KGB syndrome 1 1 Marianne Vos (LOVD-team)
00039395 - PubMed: Bosch 2016, Journal: Bosch 2016 - F no Netherlands - - - - - CVI, ID - 1 1 Danielle Bosch
00111391 S_078 PubMed: Popp 2017, Journal: Popp 2017 - M no - - - - - - XIGIS;MRD25 Severe ID, behavioral anomalies, scoliosis, hernia, strabismus, short stature, microcephaly 1 1 Bernt Popp
00154964 - - - M - (Germany) - - - - - ? Global developmental delay (HP:0001263); Muscular hypotonia (HP:0001252); Strabismus (HP:0000486); Poor speech (HP:0002465) 1 1 IMGAG
00226093 03216 - - F yes (Turkey) Kurdish 02y - - - XIGIS;MRD25 global developmental delay (HP:0001263), hypoplasia corpus callosum (HP:0002079), laryngomalacia (HP:0001601), lack of speech (HP:0001344) 1 1 Evren Gumus
00234329 XG_F - - M ? Brazil - 14y - - - XIGIS;MRD25 convulsion, neurovelopmental disease, sleep apnea 1 1 Augusto César Cardoso-dos-Santos
00289813 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00289814 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00289815 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00289816 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 12 Mohammed Faruq
00306245 - - - F - - - - - - - ? Global developmental delay (HP:0001263); Recurrent infections (HP:0002719); Short stature (HP:0004322) 1 1 IMGAG
00316019 PatRGP_79 DiTroia ASHG2020 2-generation family, 1 affected M - United States - - - - - ? developmental delay, hypotonia, scoliosis, inverted nipples, webbed toes, hypermobility 1 1 Johan den Dunnen
00401639 197P - - M no Spain - - - - - ID - 1 1 Alejandro Brea-Fernández
00408818 196079 - - F no Germany - - - - - XIGIS;MRD25 Bilateral tonic-clonic seizure, Generalized non-motor (absence) seizure, Global developmental delay, Neurodevelopmental delay 1 1 Andreas Laner
00410019 - - - F no - - - - - - XIGIS;MRD25 - 1 1 Stefano Giuseppe Caraffi
00440400 PED3489.1 PubMed: Nambot 2018 - - - France - - - - - ? - 1 1 Johan den Dunnen
00448183 Pat32 PubMed: Poli 2024 - M - Chile - - - - - ? intellectual disability; microcephaly; minor facial anomalies; scoliosis; renal tubular acidosis; poikiloderma 1 1 Johan den Dunnen
00449868 - - - F - - - - - - - SCZD Neonatal hypotonia, Delayed speech and language development, Scoliosis, Schizophrenia, Unilateral renal agenesis 1 1 Camille Verebi
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