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204394002: Congenital anomaly of myocardium (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
313423015 Congenital anomaly of myocardium en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
589613011 Congenital anomaly of myocardium (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4880301000241111 anomalie congénitale du myocarde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

25 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital anomaly of myocardium Is a Congenital heart disease true Inferred relationship Some
Congenital anomaly of myocardium Occurrence Congenital false Inferred relationship Some
Congenital anomaly of myocardium Finding site Cardiac internal structure false Inferred relationship Some 1
Congenital anomaly of myocardium Associated morphology anomalie congénitale false Inferred relationship Some 1
Congenital anomaly of myocardium Finding site Structure of cardiovascular system subdivision (body structure) false Inferred relationship Some 2
Congenital anomaly of myocardium Finding site Structure of cardiovascular system (body structure) false Inferred relationship Some 2
Congenital anomaly of myocardium Is a Structural disorder of heart (disorder) false Inferred relationship Some
Congenital anomaly of myocardium Is a Viscus structure finding (finding) false Inferred relationship Some
Congenital anomaly of myocardium Is a Congenital anomaly of trunk false Inferred relationship Some
Congenital anomaly of myocardium Is a Congenital anomaly of cardiovascular system false Inferred relationship Some
Congenital anomaly of myocardium Is a Myocardial lesion false Inferred relationship Some
Congenital anomaly of myocardium Is a Myocardial disease true Inferred relationship Some
Congenital anomaly of myocardium Finding site Myocardium structure false Inferred relationship Some 1
Congenital anomaly of myocardium Finding site Myocardium structure true Inferred relationship Some 1
Congenital anomaly of myocardium Associated morphology anomalie congénitale false Inferred relationship Some 1
Congenital anomaly of myocardium Occurrence Congenital false Inferred relationship Some 2
Congenital anomaly of myocardium Associated morphology anomalie du développement false Inferred relationship Some 2
Congenital anomaly of myocardium Finding site Myocardium structure false Inferred relationship Some 2
Congenital anomaly of myocardium Occurrence Congenital true Inferred relationship Some 1
Congenital anomaly of myocardium Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital anomaly of myocardium Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital heart block Is a False Congenital anomaly of myocardium Inferred relationship Some
Endocardial fibroelastosis unassociated with other cardiac abnormalities. Is a False Congenital anomaly of myocardium Inferred relationship Some
Congenital stenosis of mitral valve Is a False Congenital anomaly of myocardium Inferred relationship Some
Congenital absence of papillary muscle Is a False Congenital anomaly of myocardium Inferred relationship Some
Anomalous cardiac muscle bands Is a True Congenital anomaly of myocardium Inferred relationship Some
Parachute malformation of tricuspid valve Is a False Congenital anomaly of myocardium Inferred relationship Some
Fused mitral papillary muscles Is a True Congenital anomaly of myocardium Inferred relationship Some
Hypoplastic mitral papillary muscle Is a False Congenital anomaly of myocardium Inferred relationship Some
Congenital absence of right atrioventricular valve papillary muscle (disorder) Is a False Congenital anomaly of myocardium Inferred relationship Some
Congenital fusion of right atrioventricular valve papillary muscles Is a False Congenital anomaly of myocardium Inferred relationship Some
Primary endocardial fibroelastosis of left ventricle Is a False Congenital anomaly of myocardium Inferred relationship Some
Congenital supravalvular mitral stenosis Is a False Congenital anomaly of myocardium Inferred relationship Some
Hypoplasia of trabecular portion of right ventricle (disorder) Is a True Congenital anomaly of myocardium Inferred relationship Some
Congenital abnormality of tricuspid papillary muscle (disorder) Is a True Congenital anomaly of myocardium Inferred relationship Some
Congenital abnormality of atrioventricular valve papillary muscle in atrioventricular septal defect (disorder) Is a False Congenital anomaly of myocardium Inferred relationship Some
Congenital abnormality of right atrioventricular valve papillary muscle in double inlet ventricle (disorder) Is a False Congenital anomaly of myocardium Inferred relationship Some
Hypoplasia of trabecular portion of left ventricle (disorder) Is a True Congenital anomaly of myocardium Inferred relationship Some
Absent mitral papillary muscle Is a True Congenital anomaly of myocardium Inferred relationship Some
Uhl's disease Is a True Congenital anomaly of myocardium Inferred relationship Some
Cardiomyopathy and renal anomaly syndrome (disorder) Is a True Congenital anomaly of myocardium Inferred relationship Some
Cardiomyopathy-hypotonia-lactic acidosis syndrome is characterized by 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 nonconsanguineous Turkish family. The syndrome is caused by a homozygous point mutation in the exon 3A of the SLC25A3 gene encoding a mitochondrial membrane transporter. Is a True Congenital anomaly of myocardium Inferred relationship Some
A rare autosomal dominant form of heart-hand syndrome that is characterized by adult onset, progressive cardiac conduction disease, tachyarrhythmias that can lead to sudden death, dilated cardiomyopathy and brachydactyly, with the hands less severely affected than the feet. Muscle weakness and/or myopathic electromyographic findings have been observed in some cases. Is a True Congenital anomaly of myocardium Inferred relationship Some
Congenital cataract - hypertrophic cardiomyopathy - mitochondrial myopathy (CCM) is a mitochondrial disease characterized by cataracts, hypertrophic cardiomyopathy, muscle weakness and lactic acidosis after exercise. Is a True Congenital anomaly of myocardium Inferred relationship Some
A rare arrhythmogenic right ventricular cardiomyopathy (ARVC) and a cutaneous phenotype, characterized by peculiar wooly hair and palmoplantar keratoderma. Is a True Congenital anomaly of myocardium Inferred relationship Some
This syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH). Is a True Congenital anomaly of myocardium Inferred relationship Some
A rare glycogen storage disease characterized by fetal or neonatal onset of severe cardiomyopathy with non-lysosomal glycogen accumulation and fatal outcome in infancy. Patients present with massive cardiomegaly, severe cardiac and respiratory complications, and failure to thrive. Non-specific facial dysmorphism, bilateral cataracts, macroglossia, hydrocephalus, enlarged kidneys, and skeletal muscle involvement have been reported in some cases. Is a True Congenital anomaly of myocardium Inferred relationship Some

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