Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module | Reference Sets |
3313307010 | Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | GB English: Preferred (foundation metadata concept) |
3313308017 | Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | GB English: Preferred (foundation metadata concept) |
3313306018 | This syndrome has characteristics of hypertrophic cardiomyopathy, muscular hypotonia and the presence of lactic acidosis at birth. It has been described in two sisters (both of whom died within the first year of life) from a non-consanguineous Turkish family. The syndrome is caused by a homozygous point mutation in the exon 3A of the SLC25A3 gene encoding a mitochondrial membrane transporter. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core | GB English: Preferred (foundation metadata concept) |
3935221000052118 | syndrom med hypertrofisk kardiomyopati, hypotoni och laktacidos | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) | Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Due to | Mitochondrial cytopathy (disorder) | true | Inferred relationship | Some | 3 | |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Is a | Congenital anomaly of skeletal muscle | true | Inferred relationship | Some | ||
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Is a | Lactic acidosis | true | Inferred relationship | Some | ||
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Is a | Hypertrophic mitochondrial cardiomyopathy (disorder) | true | Inferred relationship | Some | ||
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Associated morphology | Developmental anomaly (morphologic abnormality) | false | Inferred relationship | Some | 3 | |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 3 | |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Associated morphology | Hypertrophy | false | Inferred relationship | Some | 4 | |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Finding site | Myocardium structure | false | Inferred relationship | Some | 4 | |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Is a | Congenital cardiovascular disorder (disorder) | false | Inferred relationship | Some | ||
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Is a | Congenital anomaly of myocardium | true | Inferred relationship | Some | ||
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Associated morphology | Hypertrophy | true | Inferred relationship | Some | 2 | |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Finding site | Myocardium structure | true | Inferred relationship | Some | 2 | |
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets