All individuals with variants in gene SLC9A3

2 entries on 1 page. Showing entries 1 - 2.
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     
00000208 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), no prolactin deficiency, age sonographic determination testicular volume 17.64y, testicular volume right/left 21/20 (7.3–16ml) 1 1 Yu Sun
00435629 Pat1 PubMed: Morleo 2023 2-generation family, 1 affected, unaffected non-carrier parents M no Kazakhstan - - - - - NDD see paper; ..., motor delay, 5y-walk; no speech; intellectual disability; no seizures; mild optic atrophy; hypotonia; MRI brain abnormal lateral ventricles (contour), abnormal white matter signal, Chiari malformation type 1 (s/p repair); coronal synostosis, mildly tapered fingers, 5th finger clinodactyly; prominent maxilla/upper lip; no micrognathia; long ears 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.