All individuals with variants in gene WDR72

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     
00291267 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 88 Mohammed Faruq
00304473 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00304474 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00385881 V1.14 PubMed: Prasad 2016 - M - - - - - - - AI isolated hypoplastic, hypomineralised amelogenesis imperfecta 2 1 Johan den Dunnen
00444045 PID_13 PubMed: Sarker 2023 family history M - Bangladesh - - - - - DMD no calf hypertrophy; Gower sign positive; normal CPK level; no feeding difficulties; no toe walking; poor walking/running ability; no difficulty climbing stairs; no waddling feet/gait; no seizure; no muscle weakness; no skinny legs/arms; normal developmental milestones; no intellectual disability; no delayed speech; not hyperactive 1 1 Johan den Dunnen
00469891 - PubMed: Jacob 2025 2-generation family, 1 affected, unaffected heterozygous carrier parents - - India - - - - - skeletal dysplasia - 1 1 Johan den Dunnen
Legend   How to query  


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