Disease #02336 (Brody myopathy (myopathy, Brody), OMIM:601003)

Official abbreviation Brody myopathy
Name myopathy, Brody
OMIM ID 601003
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene ATP2A1
Associated tissues -
Disease features autosomal recessive
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

3 entries on 1 page. Showing entries 1 - 3.
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     
00204197 - - - M no Portugal - - - - - Brody myopathy impaired/prolongued muscle relaxation upon vigorous contraction ATP2A1 ATP2A1 1 1 Luis Braz
00361991 Pat13 PubMed: Saat 2021 - M yes - - - - - - Brody myopathy Muscle weakness HP:0001324 Hypotonia HP:0001252 - ATP2A1 1 1 Ibrahim Sahin
00436399 269467 - - M no Germany - - - - - Brody myopathy Myopathy ATP2A1 ATP2A1 2 1 Andreas Laner
Legend   How to query  


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