Dilated Cardiomyopathy-1C

Preferred Label : Dilated Cardiomyopathy-1C;

NCIt synonyms : CMD1C;

NCIt definition : An autosomal dominant subtype of dilated cardiomyopathy caused by mutation(s) in the LDB3 gene, encoding LIM domain-binding protein 3.;

Details

Origin ID

C170436;

UMLS CUI

C1832244;

Currated CISMeF NLP mapping
- Cardiomyopathy, dilated, 1c, with or without left ventricular noncompaction [OMIM Phenotype]
- cardiomyopathy, dilated, 1C [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1C [MeSH concept]
- dilated cardiomyopathy 1C [DO Concept]
Excludes anatomical site(s)
- Bone [NCIt concept]
Has associated anatomic sites
- Cardiovascular System [NCIt concept]
- Connective and Soft Tissue [NCIt concept]
- Heart [NCIt concept]
- Musculoskeletal System [NCIt concept]
- Respiratory System [NCIt concept]
- Thoracic Cavity [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cardiomyopathy, dilated, 1c, with or without left ventricular noncompaction [OMIM Phenotype]
- cardiomyopathy, dilated, 1C [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1C [MeSH concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
- Soft Tissue [NCIt concept]
disease_mapped_to_gene
- LDB3 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients