All individuals with variants in gene FOXE1

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00358834 HC-266 PubMed: Alcántara-Ortigoza 2021 - F no Mexico Mexican - - yes Thyroid hormone supplementation CHNG2 Patient diagnoses as congenital hypothyroidism by newborn screening. Thyroid agenesis diagnosed by ultrasonography. 1 1 Miguel Angel Alcántara-Ortigoza
00358835 HC-215 PubMed: Alcántara-Ortigoza 2021 - F no Mexico Mexican - - yes Thyroid hormone supplementation CHNG2 Congenital hypothyroidism due to thyroid ectopy diagnosed by scintigraphy. 1 1 Miguel Angel Alcántara-Ortigoza
00426635 ? PubMed: Peng 2016 - - - Taiwan Taiwanese - - - - OFC bilateral cleft lip with palate 1 1 LOVD
00426636 ? PubMed: Peng 2016 - - - Taiwan Taiwanese - - - - OFC bilateral cleft lip with palate 1 1 LOVD
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.