Disease #01227 (CMD1A (cardiomyopathy, dilated, type 1A (CMD-1A)), OMIM:115200)

Official abbreviation CMD1A
Name cardiomyopathy, dilated, type 1A (CMD-1A)
OMIM ID 115200
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene LMNA
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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00029036 MC131 PubMed: El Malti 2016, Journal: El Malti 2016 - M no France European >57y - yes implantable cardiac defibrillator CHTD4, CMD1A congestive heart failure, secundum atrial septal defect third degree atrioventricular block cataract pectus excavatum - NKX2-5 1 1 Patrice Bouvagnet
00452319 A-IV-6 Journal: Ranta-aho 2024 - M ? United States - - - - - CMD1A, MPD6 HP:0009027, HP:0002460 - ACTN2 1 4 Johanna Ranta-aho
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