Disease #01458 (DM1 (dystrophy, myotonic, type 1 (DM-1, Steinert disease)), OMIM:160900)

Official abbreviation DM1
Name dystrophy, myotonic, type 1 (DM-1, Steinert disease)
OMIM ID 160900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 1 gene DMPK
Associated tissues -
Disease features -
Remarks autosomal dominant
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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     
00464529 - Swinkels et al. 2025, submitted - M - Netherlands - - - - - DM1 - DMPK DMPK 1 1 Hilde Swinkels
00464544 - Swinkels et al. 2025, submitted - M - Netherlands - - - - - DM1 - DMPK DMPK 1 1 Hilde Swinkels
00464618 - Swinkels et al. 2025, submitted - M - Netherlands - - - - - DM1 - DMPK DMPK 1 1 Hilde Swinkels
00464619 - Swinkels et al. 2025, submitted - M - Netherlands - - - - - DM1 - DMPK DMPK 1 1 Hilde Swinkels
00464620 - Swinkels et al. 2025, submitted - M - Netherlands - - - - - DM1 - DMPK DMPK 1 1 Hilde Swinkels
00464621 - Swinkels et al. 2025, submitted - F - Netherlands - - - - - DM1 - DMPK DMPK 1 1 Hilde Swinkels
Legend   How to query  


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