Disease #05805 (RHDA (hypodysplasia/aplasia, renal (RHDA)))

Official abbreviation RHDA
Name hypodysplasia/aplasia, renal (RHDA)
OMIM ID -
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene GREB1L
Associated tissues -
Disease features -
Remarks -
Date created 2020-08-07 09:59:48 +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     
00307269 family 3-generation family, 4 affected (F, 2M, fetus) - F;M - China - - - - - RHDA see paper; ... GREB1L GREB1L 1 1 Johan den Dunnen
Legend   How to query  


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