Disease #07055 (BRYLIB (Bryant-Li-Bhoj neurodevelopmental syndrome))

Official abbreviation BRYLIB
Name Bryant-Li-Bhoj neurodevelopmental syndrome
OMIM ID -
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 2 genes H3F3A, H3F3B
Associated tissues -
Disease features -
Remarks -
Date created 2023-12-24 13:24:41 +01:00 (CET)
Date last edited N/A


Individuals

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00465870 331975 - - M ? Syria - - - - - BRYLIB Delayed speech and language development, Neurodevelopmental delay, Delayed gross motor development, Overlapping toe, Abnormal cheek morphology, Abnormal skin morphology, Downslanted palpebral fissures, Gingival overgrowth H3F3A H3F3A 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.