Disease #03289 (FSGS5 (glomerulosclerosis, segmental, focal, type 5 (FSGS-5)), OMIM:613237)

Official abbreviation FSGS5
Name glomerulosclerosis, segmental, focal, type 5 (FSGS-5)
OMIM ID 613237
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene INF2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
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     
00301048 - PubMed: Büscher 2018 4-generation family, 14 affected (6F, 8M) M no Germany - 44y - - - FSGS5 - ACTN4, CD2AP, COQ6, INF2, LAMB2, NPHS1, NPHS2, PLCE1, TRPC6, WT1 ACTN4, INF2 2 7 Matthias Braunisch
Legend   How to query  


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