All individuals with variants in gene NBEA

5 entries on 1 page. Showing entries 1 - 5.
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     
00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 1 1 Yu Sun
00229654 - - - M - - - - - - - ? Global developmental delay (HP:0001263); Myoclonic atonic seizures (HP:0011170); Generalized-onset seizure (HP:0002197); Status epilepticus (HP:0002133) 1 1 IMGAG
00325363 - - - M - - - - - - - ? Behavioral abnormality (HP:0000708); Muscular hypotonia (HP:0001252); Global developmental delay (HP:0001263); Absent speech (HP:0001344) 1 1 IMGAG
00448490 286203 - - M no ? (unknown) - - - - - MR;ID Autistic behavior, Absent speech, Abnormal repetitive mannerisms, Reduced eye contact, seizures 1 1 Andreas Laner
00462236 200654 - - M no ? (unknown) - - - - - NEDEGE Global developmental delay, Slurred speech 1 1 Andreas Laner
Legend   How to query  


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