Disease #05915 (TBHS (hypertelorism, Teebi type syndrome (TBHS)))

Official abbreviation TBHS
Name hypertelorism, Teebi type syndrome (TBHS)
OMIM ID -
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SPECC1L
Associated tissues -
Disease features -
Remarks -
Date created 2021-04-06 19:13:17 +02:00 (CEST)
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     
00446571 - - - F no Spain Spain - - - - TBHS hypertelorism (HP:0000316); omphalocele (HP:0001539); bicornuate uterus (HP:0000813); congenital diaphragmatic hernia (HP:0000776) - SPECC1L 1 1 Maria Elena García Paya
Legend   How to query  


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