Disease #02481 (CMD1G (cardiomyopathy, dilated, type 1G (CMD-1G)), OMIM:604145)

Official abbreviation CMD1G
Name cardiomyopathy, dilated, type 1G (CMD-1G)
OMIM ID 604145
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene TTN
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

2 entries on 1 page. Showing entries 1 - 2.
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00373333 family large 3-generation family, 10 affected - F no Malta white - - - - CMD1G Proband of family with dilated cardiomyopathy (HP:0001644); mother died of congestive heart failure (HP:0001635) TTN TTN 1 10 Laboratory of Molecular Genetics
00411324 - - - M no Thailand - - - - - CMD1G - - TTN 1 1 Ponghatai Damrongphol
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