All individuals with variants in gene ADAMTS18

12 entries on 1 page. Showing entries 1 - 12.
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     
00001384 - - - - - - - - - - - MMCAT - 1 4 Anas M Alazami
00001390 - PubMed: Aldahmesh 2011 2-generation faily, 1 affected F yes Saudi Arabia - >08y - - - KNO2 after birth occipital meningocoele noted, brain CT normal; normal cognitive/motor development; 18m-poor vision; ectopia lentis, cataract (left eye), retinal degeneration, serous retinal detachment (left eye), high myopia; occipital encephalocele, developmental delay 1 1 Johan den Dunnen
00001391 - - 2-generation family, unafected carrier parents/sibling - - Saudi Arabia - - - - - Healthy/Control - 2 3 Johan den Dunnen
00001394 - - - - - - - - - - - MMCAT - 1 4 Anas M Alazami
00001395 - - - - - - - - - - - MMCAT - 1 4 Anas M Alazami
00001396 - - - - - - - - - - - MMCAT - 1 4 Anas M Alazami
00334450 RP-071 PubMed: Huang 2017 patient - - China - - - - - retinal disease see paper; ... 2 1 LOVD
00363750 14DG1964 PubMed: Patel 2016 - - - Saudi Arabia - - - - - retinal disease syndromic 1 1 LOVD
00379704 R0017 PubMed: Wan 2018 - ? - China Han Chinese - - - - retinal disease - 1 1 LOVD
00383406 - PubMed: Khan 2019 - M - - - - - - - retinal disease - 1 1 LOVD
00386168 RPN-278 PubMed: Rodriguez-Munoz 2020 - ? - Spain - - - - - retinal disease - 1 1 LOVD
00386278 RPN-179 PubMed: Rodriguez-Munoz 2020 - ? - Spain - - - - - retinal disease - 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.