FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

74281007: Myocardium structure (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
123357010 Myocardium en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
123359013 Cardiac muscle en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
502654017 Myocardium structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
814763019 Myocardium structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
12751000077119 structure du myocarde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
885351000172119 myocarde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
891301000172115 myocardium fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
949031000172111 structure myocardique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


175 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myocardium structure Is a Cardiac wall structure true Inferred relationship Some
Myocardium structure partie de Entire heart false Additional relationship Some
Myocardium structure Is a Structure of striated muscle true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Implantation of blood vessels into myocardium Procedure site - Indirect (attribute) True Myocardium structure Inferred relationship Some 2
Aorto-myocardial shunt Procedure site - Indirect (attribute) False Myocardium structure Inferred relationship Some 4
Erythrokeratodermia-cardiomyopathy syndrome is a rare, genetic erythrokeratoderma disorder characterized by generalized cutaneous erythema with fine white scales and pruritus refractory to treatment, progressive dilated cardiomyopathy, palmoplantar keratoderma, sparse or absent eyebrows and eyelashes, sparse scalp hair, nail dystrophy, and dental enamel anomalies. Variable features include failure to thrive, developmental delay, and development of corneal opacities. Histology shows psoriasiform acanthosis, hypogranulosis, and compact orthohyperkeratosis. Finding site True Myocardium structure Inferred relationship Some 1
A rare mitochondrial disease characterized by neonatal onset of severe cardiac and/or neurologic signs and symptoms mostly associated with a fatal outcome in the neonatal period or in infancy, although a milder phenotype with later onset and slowly progressive neurologic deterioration has also been reported. Clinical manifestations are variable and include respiratory insufficiency, hypotonia, cardiomyopathy, and seizures. Serum lactate is elevated in most cases. Brain imaging may show cerebellar atrophy or hypoplasia. Finding site True Myocardium structure Inferred relationship Some 1
Cardiomyopathy due to acromegaly (disorder) Finding site True Myocardium structure Inferred relationship Some 1
Maternally inherited mitochondrial cardiomyopathy (disorder) Finding site True Myocardium structure Inferred relationship Some 1
A rare mitochondrial disease characterized by prenatal or early infantile onset of severe cardiomyopathy, failure to thrive and global developmental delay, sensorineural hearing loss, and severe lactic acidosis. Hepatic involvement and adrenal insufficiency, as well as encephalopathy and anomalies of deep gray matter structures on brain MRI have also been reported. Finding site True Myocardium structure Inferred relationship Some 1
Myocardial dysfunction with sepsis (disorder) Finding site True Myocardium structure Inferred relationship Some 2
Subsequent anterior non-ST segment elevation myocardial infarction (disorder) Finding site True Myocardium structure Inferred relationship Some 3
Myocarditis due to idiopathic hypereosinophilic syndrome Finding site True Myocardium structure Inferred relationship Some 1
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. Finding site True Myocardium structure Inferred relationship Some 1
Dilated cardiomyopathy caused by ethanol (disorder) Finding site True Myocardium structure Inferred relationship Some 1
Replacement of electronic heart device, myocardial electrode Procedure site - Indirect (attribute) True Myocardium structure Inferred relationship Some 1
Dilated cardiomyopathy due to scleroderma (disorder) Finding site True Myocardium structure Inferred relationship Some 1
Acute ST segment elevation myocardial infarction due to occlusion of proximal portion of circumflex branch of left coronary artery (disorder) Finding site True Myocardium structure Inferred relationship Some 1
Acute ST segment elevation myocardial infarction due to distal left circumflex coronary artery occlusion Finding site True Myocardium structure Inferred relationship Some 1
Acute ST segment elevation myocardial infarction due to obtuse marginal branch of left circumflex coronary artery occlusion Finding site True Myocardium structure Inferred relationship Some 1
Acute ST segment elevation myocardial infarction due to posterolateral branch of left circumflex coronary artery occlusion Finding site True Myocardium structure Inferred relationship Some 1
Acute ST segment elevation myocardial infarction due to mid left circumflex coronary artery occlusion Finding site True Myocardium structure Inferred relationship Some 1
A rare inborn error of metabolism characterized by massive accumulation of triglycerides in the myocardium and coronary arteries, while plasma triglyceride levels are normal. Patients present in adulthood with signs and symptoms of coronary artery disease and severe heart failure. Concomitant skeletal myopathy is common. Vacuole formation in polymorphonuclear leukocytes is typically observed. Finding site True Myocardium structure Inferred relationship Some 2
Toxic dilated cardiomyopathy (disorder) Finding site True Myocardium structure Inferred relationship Some 1
Toxic cardiomyopathy Finding site True Myocardium structure Inferred relationship Some 1
Transient myocardial ischaemia Finding site True Myocardium structure Inferred relationship Some 1
Prinzmetal angina Finding site True Myocardium structure Inferred relationship Some 1
Aorto-myocardial shunt Procedure site - Direct (attribute) True Myocardium structure Inferred relationship Some 2
Structure of myocardium of apex of heart Is a True Myocardium structure Inferred relationship Some
Type 5 myocardial infarction (disorder) Finding site True Myocardium structure Inferred relationship Some 1
Structure of myocardium of cardiac septum Is a True Myocardium structure Inferred relationship Some
Eosinophil infiltration of myocardium (finding) Finding site True Myocardium structure Inferred relationship Some 1
An early-onset and most severe form of rare haemochromatosis characterised by the usual features of haemochromatosis accompanied by cardiomyopathy and hypogonadism. Finding site True Myocardium structure Inferred relationship Some 3
Type 2A juvenile hereditary hemochromatosis (disorder) Finding site True Myocardium structure Inferred relationship Some 3
Type 2B juvenile hereditary hemochromatosis Finding site True Myocardium structure Inferred relationship Some 3
Angina pectoris due to microvascular ischemia of myocardium (disorder) Finding site True Myocardium structure Inferred relationship Some 1
Acute microvascular ischemia of myocardium Finding site True Myocardium structure Inferred relationship Some 1
Angina pectoris due to arteriosclerosis of nonautologous biological coronary artery bypass graft (disorder) Finding site True Myocardium structure Inferred relationship Some 2
Myocardial ischemia due to coronary arteriosclerosis Finding site True Myocardium structure Inferred relationship Some 1
Chronic microvascular ischemia of myocardium (disorder) Finding site True Myocardium structure Inferred relationship Some 1

Start Previous Page 12 of 12


Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

Back to Start