All individuals with variants in gene TNFRSF11A

3 entries on 1 page. Showing entries 1 - 3.
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     
00050538 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? microcephaly, muscular hypotonia, short philtrum, upslanted palpebral fissure 1 1 Johan den Dunnen
00359411 Pat55 PubMed: Silveira 2021, Journal: Silveira 2021 - F ? Brazil - - - - - OPTB7 - 1 1 Maria Dora Jazmin Lacarrubba-Flores
00408098 169 PubMed: Alabdullatif 2017 - M yes United Arab Emirates - - - - - retinal disease 1.5 year old boy with an uncomplicated perinatal course. At the age of 2 months, he was noticed to have plugging anterior fontanel. Brain MRI showed subdural hygroma with enlarger subarachnoid space, and he was diagnosed with external hydrocephalus that required taping twice. In addition, he had developmental delay, bilateral optic atrophy, epilepsy, short stature, failure to thrive, and distinctive facial features (prominent forehead, small nose, and micro-retrognathia). Skeletal survey at the age of 2 months showed diffuse sclerosis of the all the axial and peripheral skeleton with loss of corticomedullary differentiation consistent with osteopetrosis. His parents were cousins, and he was the first child for them. 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.