Disease #00082 (JBTS9 (Joubert syndrome, type 9 (JBTS-9)), OMIM:612285)

Official abbreviation JBTS9
Name Joubert syndrome, type 9 (JBTS-9)
OMIM ID 612285
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CC2D2A
Associated tissues -
Disease features -
Remarks -
Date created 2012-11-09 15:25:03 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


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     
00431162 - - - F no Italy - - - - - JBTS9 - CC2D2A CC2D2A 2 1 Domenico Coviello
Legend   How to query  


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