All individuals with variants in gene ALG3

6 entries on 1 page. Showing entries 1 - 6.
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     
00081089 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - CDG1D Congenital disorder of glycosylation, type Id (OMIM:601110) 1 1 Daniel Trujillano
00249657 - - - ? - Germany - - - - - CDG1D - 1 1 Gert Matthijs
00275637 FamMR82Pat3 PubMed: Santos-Cortez 2018 4-generation family, 2 affected (2M), unaffected heterozygous carrier parents/relatives M yes Pakistan - - - - - ID OFC 50cm; IQ 45, moderate intellectual disability (HP:0002342); poor speech, seizures 1 2 Johan den Dunnen
00275638 FamMR82Pat4 PubMed: Santos-Cortez 2018 - M yes Pakistan - - - - - ID OFC 49cm; IQ 45, moderate intellectual disability (HP:0002342) 1 1 Johan den Dunnen
00293290 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 44 Mohammed Faruq
00304941 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
Legend   How to query  


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