Disease #05463 (trichromacy (trichromacy, oligocone))

Official abbreviation trichromacy
Name trichromacy, oligocone
OMIM ID -
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene CEP290
Associated tissues -
Disease features -
Remarks -
Date created 2018-07-30 21:10:25 +02:00 (CEST)
Date last edited N/A


Individuals

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     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00117374 28829391-FamPat1 PubMed: Roosing 2017 family, two affected siblings, hetorozygous carrier parents F ? Netherlands white - - yes none trichromacy see paper; ... CEP290 CEP290 2 2 Susanne Roosing
00117375 28829391-FamPat2 PubMed: Roosing 2017 sibling M no Netherlands white - - - none trichromacy see paper; ... CEP290 CEP290 2 1 Susanne Roosing
Legend   How to query  


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