Disease #03225 (EDMD5 (dystrophy, muscular, Emery-Dreifuss, type 5, autosomal dominant (EDMD-5)), OMIM:612999)

Official abbreviation EDMD5
Name dystrophy, muscular, Emery-Dreifuss, type 5, autosomal dominant (EDMD-5)
OMIM ID 612999
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene SYNE2
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

5 entries on 1 page. Showing entries 1 - 5.
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     
00079584 - PubMed: Zhang 2007 Fam2 M - (United Kingdom (Great Britain)) - - - - - EDMD5 muscular dystrophy, severe dilated cardiomyopathy requiring heart transplantation 26y SYNE1 SYNE1, SYNE2 2 1 Johan den Dunnen
00079623 - PubMed: Zhang 2007 Fam4. mother of G-11774 F - (United Kingdom (Great Britain)) - - - - - EDMD5 - SYNE2 SYNE2 1 1 Johan den Dunnen
00079624 - PubMed: Zhang 2007 Fam4 F - (United Kingdom (Great Britain)) - - - - - EDMD5 - SYNE2 SYNE2 1 1 Johan den Dunnen
00079625 - PubMed: Zhang 2007 Fam4, father of G-9951, G-9539 M - (United Kingdom (Great Britain)) - - - - - EDMD5 - SYNE2 SYNE2 1 1 Johan den Dunnen
00079626 - PubMed: Zhang 2007 Fam4 M - (United Kingdom (Great Britain)) - - - - - EDMD5 - SYNE2 SYNE2 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.