All individuals with variants in gene CUX2

5 entries on 1 page. Showing entries 1 - 5.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00154932 - - - F no Denmark - - - - - epilepsy, ID pregnancy uneventful; moderate intellectual disability (HP:0002342); moderate global developmental delay (HP:0011343); severe speech delay (HP:0000750) 1 1 Elsebet Østergaard
00380400 Pat5 PubMed: Goodman 2021, Journal: Goodman 2021 - - - Australia - - - - - NDD global developmental delays; speech impaired; motor impaired; no dysmorphic features; no behavioral deficits; GI/feeding abnormalities; ophthalmologic abnormalities; hypotonia muscle; movement/neurological disorder; no seizures; microcephaly; MRI brain abnormalities 1 1 Johan den Dunnen
00427665 202469 - - M no Germany - - - - - EIEE67 Talipes equinovarus, Neonatal seizure, Neonatal hypotonia, Temperature instability 1 1 Andreas Laner
00433665 - - - - - - - - - - - DEE mild intellectual disability, autism, speech delay, hyperactivity 1 1 Marketa Wayhelova
00438372 Pat90 PubMed: Chuan 2022 - F - China - - - - - epilepsy HP:0001250 seizures 1 1 Johan den Dunnen
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