All individuals with variants in gene DCHS1

10 entries on 1 page. Showing entries 1 - 10.
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AscendingIndividual ID     

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00065133 SIDS061 PubMed: Neubauer 2017 Journal: Neubauer 2017 - M ? Switzerland Europe 00y04m - - - SIDS SIDS 1 1 Cordula Haas
00065155 SIDS223 PubMed: Neubauer 2017 Journal: Neubauer 2017 - F ? Switzerland Europe 00y02m - - - SIDS SIDS 1 1 Cordula Haas
00103747 SUDS049 PubMed: Neubauer 2018, Journal: Neubauer 2018 - M - Switzerland Europe 22y - - - SUD SUD 1 1 Cordula Haas
00290493 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 6 Mohammed Faruq
00316096 K13 PubMed: Heidet 2017 fetus - - France - - - - - CAKUT bilateral multicystic dysplasia 1 1 Johan den Dunnen
00316111 K159 PubMed: Heidet 2017 - - - France - - - - - CAKUT renal dysplasia; cysts; unilateral kidney agenesis 1 1 Johan den Dunnen
00316166 K60 PubMed: Heidet 2017 fetus - - France - - - - - CAKUT renal dysplasia; cysts; pancreas hypoplasia 1 1 Johan den Dunnen
00316182 K86 PubMed: Heidet 2017 - - - France - - - - - CAKUT unilateral multicystic dysplasia; vesico-ureteral reflux; morning glory syndrome, intellectual disability 1 1 Johan den Dunnen
00390710 187442 - - M no Germany - - - - - NDD Global developmental delay, Neurodevelopmental delay, Intellectual disability, Seizure, Focal motor seizure, Arthrogryposis multiplex congenita, Spinal dysplasia, Abnormal palate morphology, Abnormality of the dentition, Abnormality of dental morphology, Telecanthus, Tracheomalacia, Abnormality of the outer ear, Abnormality of the pinna, Abnormality of finger, Abnormality of the genitourinary system, Gonadal dysgenesis, Abnormal external genitalia, Abnormal internal genitalia, Anal atresia, Subcortical heterotopia 2 1 Andreas Laner
00413239 family PubMed: Sheffer 2015 4-generation family, 2 affected brothers, unaffected heterozygous carrier parents/relatives M yes Israel Arab;Moslem - - - - encephalopathy, neonatal, severe poor suck (HP:0002033); gastroesophageal reflux (HP:0002020); restlessness (HP:0000711); severe motor delay (HP:0001270); speech delay (HP:0000750); infantile axial hypotonia (HP:0009062); spastic tetraplegia (HP:0002510); opisthotonos (HP:0002179); cerebral visual impairment (HP:0100704); vertical nystagmus (HP:0010544); myoclonic seizures (HP:0032794); multifocal polyspike wave complexes (HP:0002392); cerebellar hypoplasia (HP:0007360); hypoplasia of the cerebellar vermis (HP:0006817); dilation of lateral and fourth ventricle (HP:0006956, HP:0002198); micrognathia (HP:0000347); high arched palate (HP:0000218); prominent metopic suture (HP:0005487); posterior bulge of the skull (HP:0000929); fisted hands (HP:0001155) 1 2 Frederike Leonie Harms
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