Familial Hypertrophic Cardiomyopathy Type 6

Preferred Label : Familial Hypertrophic Cardiomyopathy Type 6;

NCIt synonyms : CMH6;

NCIt definition : An autosomal dominant subtype of familial hypertrophic cardiomyopathy caused by mutation(s) in the PRKAG2 gene, encoding 5'-AMP-activated protein kinase subunit gamma-2.;

NCI Metathesaurus CUI : CL1643072;

Details

Origin ID

C177249;

UMLS CUI

C1833236;

Automatic exact mappings (from CISMeF team)
- hypertrophic cardiomyopathy 6 [DO Concept]
- protein kinase AMP-activated non-catalytic subunit gamma 2 [ORDO Gene]
Currated CISMeF NLP mapping
- Cardiomyopathy, familial hypertrophic, 6 [OMIM Phenotype]
- cardiomyopathy, familial hypertrophic, 6 [MeSH Supplementary Concept]
- cardiomyopathy, familial hypertrophic, 6 [MeSH 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, familial hypertrophic, 6 [OMIM Phenotype]
- cardiomyopathy, familial hypertrophic, 6 [MeSH Supplementary Concept]
- cardiomyopathy, familial hypertrophic, 6 [MeSH concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
- Soft Tissue [NCIt concept]
disease_mapped_to_gene
- PRKAG2 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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