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A dilated cardiomyopathy that has material basis in variation in the chromosome region 2q14-q22.
Features include: Enlarged and weakened heart (dilated cardiomyopathy).
Organ System | Phenotype Count | Example Features |
|---|---|---|
Heart and blood vessels | 1 | Enlarged and weakened heart (dilated cardiomyopathy) |
Biomarker and diagnostic research for dilated cardiomyopathy 1H has been reported in the published literature.
No clinical trials have been registered for dilated cardiomyopathy 1H.
10 publications have been identified in PubMed for dilated cardiomyopathy 1H. Research spans Epidemiology / Natural History (30%), Diagnostic / Biomarker (20%), and Case Report / Case Series (20%).
Research Type | Count | % of Total |
|---|---|---|
Disease patterns and progression | 3 | 30% |
Data assembled from 4 of 12 sources · Last updated Nov 2, 2026, 9:23 PM UTC
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
Testing and diagnosis research
2 |
20% |
Patient case studies | 2 | 20% |
Laboratory research | 2 | 20% |
Clinical study results | 1 | 10% |
Wu A (2026). [PMID: 41404738](https://pubmed.ncbi.nlm.nih.gov/41404738/). *Journal of the American Heart Association*. [Diagnostic / Biomarker]
Bai R (2025). [PMID: 40311326](https://pubmed.ncbi.nlm.nih.gov/40311326/). *Stem cell research*. [Basic Science / Preclinical]
Dalili M (2025). [PMID: 39432098](https://pubmed.ncbi.nlm.nih.gov/39432098/). *Pediatric cardiology*. [Clinical Trial Publication]
Gallego-Martínez A (2025). [PMID: 41126307](https://pubmed.ncbi.nlm.nih.gov/41126307/). *Clinical epigenetics*. [Epidemiology / Natural History]
Nakayama R (2025). [PMID: 39916360](https://pubmed.ncbi.nlm.nih.gov/39916360/). *ESC heart failure*. [Case Report / Case Series]
Chen H (2025). [PMID: 41276221](https://pubmed.ncbi.nlm.nih.gov/41276221/). *Virologica Sinica*. [Diagnostic / Biomarker]
Choudhary AK (2025). [PMID: 40021001](https://pubmed.ncbi.nlm.nih.gov/40021001/). *Indian heart journal*. [Epidemiology / Natural History]
Ni H (2025). [PMID: 40392911](https://pubmed.ncbi.nlm.nih.gov/40392911/). *Circulation. Heart failure*. [Epidemiology / Natural History]
Wang S (2024). [PMID: 39119584](https://pubmed.ncbi.nlm.nih.gov/39119584/). *Frontiers in genetics*. [Case Report / Case Series]
Rua AJ (2024). [PMID: 38948727](https://pubmed.ncbi.nlm.nih.gov/38948727/). *bioRxiv : the preprint server for biology*. [Basic Science / Preclinical]
AI-curated news mentioning dilated cardiomyopathy 1H
Updated Oct 12, 2026
Recent research identifies novel compound heterozygous variants in the ATAD3A gene associated with Harel-Yoon syndrome, which presents with congenital cataracts and dilated cardiomyopathy. This discovery enhances understanding of the genetic basis of this rare condition.
A recent study identifies fatal dilated cardiomyopathy and monogenic diabetes mellitus as disorders related to SMPD4 mutations. This discovery highlights the genetic underpinnings of these conditions, potentially guiding future research and therapeutic strategies.
A new study focuses on optimizing screening intervals for at-risk relatives of patients with dilated cardiomyopathy who carry TTN gene variants. This research aims to improve early detection and management strategies for familial cases of the disease.