All individuals with variants in gene NEUROD2

2 entries on 1 page. Showing entries 1 - 2.
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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     
00410464 patient PubMed: Politano 2022 - F no Italy - - - - - Rett syndrome Microcephaly Hypotonia Gait disturbance Intellectual disability Absent speech Aggressive behavior Partial agenesis of the corpus callosum Absent septum pellucidum 1 1 Edoardo Errichiello
00426138 60DF8300 PubMed: Al-Kasbi 2022 patient, no other affecteds in family M - Oman - - - - - ID - 1 1 Johan den Dunnen
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