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25322007: Dilatation (morphologic abnormality)

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
42451013 Dilatation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
42453011 Ectasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
42454017 Dilation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
42457012 Distention en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
42458019 Distension en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
755627016 Dilatation (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

54 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dilatation Is a Mechanical abnormality false Inferred relationship Some
Dilatation Is a Enlargement (morphologic abnormality) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Cardiac dilatation Associated morphology True Dilatation Inferred relationship Some 1
On examination - lateral abdominal wall veins distended Associated morphology False Dilatation Inferred relationship Some 1
On examination - chest wall veins distended Associated morphology False Dilatation Inferred relationship Some 1
Dilatation of blood vessel Associated morphology True Dilatation Inferred relationship Some 1
Abdominal wall veins distended Associated morphology True Dilatation Inferred relationship Some 1
Acute exacerbation of bronchiectasis (disorder) Associated morphology False Dilatation Inferred relationship Some 1
Acute exacerbation of bronchiectasis (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Myelocele with hydrocephalus (disorder) Associated morphology False Dilatation Inferred relationship Some 2
Dilatation of aortic sinutubular junction (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Dilatation of annulus of aortic valve (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Pulmonary vein dilatation (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Dilatation of descending aorta (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Dilatation of aortic sinus of Valsalva (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Dilation of mitral annulus (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Dilatation of pulmonary valve annulus (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Nonischemic congestive cardiomyopathy Associated morphology True Dilatation Inferred relationship Some 1
Primary dilated cardiomyopathy Associated morphology True Dilatation Inferred relationship Some 1
Left atrial dilatation Associated morphology True Dilatation Inferred relationship Some 2
Right atrial dilatation Associated morphology True Dilatation Inferred relationship Some 2
Dilatation of right cardiac ventricle (disorder) Associated morphology True Dilatation Inferred relationship Some 2
Dilatation of left cardiac ventricle (disorder) Associated morphology True Dilatation Inferred relationship Some 2
Transient ischemic dilatation of left cardiac ventricular cavity Associated morphology False Dilatation Inferred relationship Some 2
Dilatation of cardiac ventricle (disorder) Associated morphology True Dilatation Inferred relationship Some 2
Dilation of right atrioventricular (not morphologically tricuspid) valve in double inlet ventricle Associated morphology True Dilatation Inferred relationship Some 2
Dilatation of left atrioventricular (not morphologically mitral) valve in double inlet ventricle Associated morphology True Dilatation Inferred relationship Some 2
Coronary artery fistula with dilatation of proximal coronary artery and without dilatation of distal coronary artery Associated morphology True Dilatation Inferred relationship Some 3
Coronary artery fistula with dilatation of entire coronary artery Associated morphology True Dilatation Inferred relationship Some 3
Dilated cardiomyopathy with genetic marker (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Ischemic dilated cardiomyopathy due to coronary artery disease (disorder) Associated morphology True Dilatation Inferred relationship Some 3
Fetal dilated cardiomyopathy Associated morphology False Dilatation Inferred relationship Some 2
Fetal right atrial dilatation Associated morphology False Dilatation Inferred relationship Some 2
Hydrocephalus due to Arnold Chiari malformation type 2 Associated morphology True Dilatation Inferred relationship Some 3
Obstructive hydrocephalus due to and following meningitis Associated morphology True Dilatation Inferred relationship Some 1
Primary idiopathic dilated cardiomyopathy Associated morphology True Dilatation Inferred relationship Some 1
Secondary nonischemic congestive cardiomyopathy Associated morphology True Dilatation Inferred relationship Some 2
Postoperative communicating hydrocephalus Associated morphology True Dilatation Inferred relationship Some 2
Dilated cardiomyopathy 3B (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Acquired megaduodenum Associated morphology True Dilatation Inferred relationship Some 1
Megaduodenum Associated morphology True Dilatation Inferred relationship Some 1
Failure of cervical dilation due to primary uterine inertia Associated morphology False Dilatation Inferred relationship Some 2
Giant right atrium Associated morphology True Dilatation Inferred relationship Some 2
Giant left atrium Associated morphology True Dilatation Inferred relationship Some 2
Hydrocephalus associated with congenital aqueduct stenosis Associated morphology False Dilatation Inferred relationship Some 3
Aneurysm Is a True Dilatation Inferred relationship Some
Abdominal aortic ectasia (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Hydronephrosis due to ureteral stricture (disorder) Associated morphology True Dilatation Inferred relationship Some 7
Toxic megacolon due to amebic infection (disorder) Associated morphology False Dilatation Inferred relationship Some 2
Acute bronchitis co-occurrent with bronchiectasis Associated morphology True Dilatation Inferred relationship Some 4
Congenital hydronephrosis Associated morphology True Dilatation Inferred relationship Some 1
Microcephaly-cardiomyopathy syndrome is characterized by severe intellectual deficit, microcephaly and dilated cardiomyopathy. Hand and foot anomalies have also been reported. The syndrome has been described in three individuals. Transmission is autosomal recessive. Associated morphology False Dilatation Inferred relationship Some 3
Microcephaly-cardiomyopathy syndrome is characterized by severe intellectual deficit, microcephaly and dilated cardiomyopathy. Hand and foot anomalies have also been reported. The syndrome has been described in three individuals. Transmission is autosomal recessive. Associated morphology False Dilatation Inferred relationship Some 2
This syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH). Associated morphology False Dilatation Inferred relationship Some 2
Vici syndrome is a very rare and severe congenital multisystem disorder characterized by the principal features of agenesis of the corpus callosum, cataracts, oculocutaneous hypopigmentation, cardiomyopathy and combined immunodeficiency. Associated morphology True Dilatation Inferred relationship Some 7
A rare renal disease characterized by hypokalemic metabolic alkalosis secondary to a tubulopathy, hypomagnesemia with hypermagnesuria, severe hypercalciuria and dilated cardiomyopathy. Associated morphology True Dilatation Inferred relationship Some 2
A rare genetic ectodermal dysplasia syndrome characterised by woolly hair (presenting at birth), palmoplantar keratoderma (developing in the first year of life) and dilated cardiomyopathy with predominant left ventricle involvement (developing in childhood) which can lead to life-threatening heart failure in childhood or adolescence. Associated morphology True Dilatation Inferred relationship Some 5
Bilateral congenital primary hydronephrosis (disorder) Associated morphology False Dilatation Inferred relationship Some 6
Idiopathic megaesophagus (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Vascular ectasia of duodenum Associated morphology False Dilatation Inferred relationship Some 2
A rare triad of dilated cardiomyopathy, premature cataract, and articular disease of the hips and spine characterized by hip joint degeneration, irregular intervertebral discs, and platyspondyly. The ocular abnormalities are often the first symptoms to arise. There have been no further descriptions in the literature since 1985. Associated morphology True Dilatation Inferred relationship Some 4
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. Associated morphology True Dilatation Inferred relationship Some 3
Ectasia of thoracic aorta (disorder) Associated morphology True Dilatation Inferred relationship Some 1
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. Associated morphology False Dilatation Inferred relationship Some 4
Congenital hydronephrosis due to ureteropelvic junction obstruction (disorder) Associated morphology False Dilatation Inferred relationship Some 4
Acquired hydronephrosis due to urinary bladder obstruction Associated morphology False Dilatation Inferred relationship Some 3
Hydronephrosis due to bladder obstruction Associated morphology False Dilatation Inferred relationship Some 3
Hydronephrosis due to ureteral obstruction Associated morphology False Dilatation Inferred relationship Some 3
Hydronephrosis due to ureteral orifice obstruction Associated morphology False Dilatation Inferred relationship Some 3
Acquired hydronephrosis due to ureteropelvic junction obstruction (disorder) Associated morphology False Dilatation Inferred relationship Some 4
Intramucosal venous dilatation of esophagus (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Associated morphology True Dilatation Inferred relationship Some 2
Toxic megacolon due to infectious colitis (disorder) Associated morphology False Dilatation Inferred relationship Some 5
Okamoto syndrome Associated morphology False Dilatation Inferred relationship Some 9
Sensorineural deafness with dilated cardiomyopathy is an extremely rare autosomal dominant syndrome described in two families to date and characterized by moderate to severe sensorineural hearing loss manifesting during childhood and associated with late-onset dilated cardiomyopathy that generally progresses to heart failure. Associated morphology True Dilatation Inferred relationship Some 4
Cirrhotic cardiomyopathy is the term used to describe a constellation of features indicative of abnormal heart structure and function in patients with cirrhosis. These include systolic and diastolic dysfunction, electrophysiological changes, and macroscopic and microscopic structural changes. Associated morphology True Dilatation Inferred relationship Some 3
Congenital secondary hydronephrosis (disorder) Associated morphology False Dilatation Inferred relationship Some 2
This syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH). Associated morphology True Dilatation Inferred relationship Some 1
Communicating hydrocephalus due to and following traumatic hemorrhage (disorder) Associated morphology False Dilatation Inferred relationship Some 3
Myelomeningocele co-occurrent with hydrocephalus (disorder) Associated morphology False Dilatation Inferred relationship Some 9
Dilatation of gastrointestinal tract (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Hydronephrosis due to calculus of kidney and ureter (disorder) Associated morphology True Dilatation Inferred relationship Some 6
Dilatation of aortic root due to Marfan's syndrome (disorder) Associated morphology True Dilatation Inferred relationship Some 3
A rare familial cardiomyopathy characterized by left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy. Associated morphology True Dilatation Inferred relationship Some 1
Acquired megacolon in adults Associated morphology False Dilatation Inferred relationship Some 1
Toxic megacolon due to infectious colitis (disorder) Associated morphology True Dilatation Inferred relationship Some 2
Secondary acquired megacolon (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Drug-induced megacolon Associated morphology True Dilatation Inferred relationship Some 1
Acquired hydronephrosis due to ureteropelvic junction obstruction (disorder) Associated morphology True Dilatation Inferred relationship Some 2
Acquired hydronephrosis due to urinary bladder obstruction Associated morphology True Dilatation Inferred relationship Some 2
Communicating hydrocephalus due to and following traumatic hemorrhage (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Acquired obstructive hydrocephalus Associated morphology True Dilatation Inferred relationship Some 1
Cervical spina bifida with hydrocephalus - open Associated morphology True Dilatation Inferred relationship Some 3
Cervical spina bifida with hydrocephalus - closed Associated morphology True Dilatation Inferred relationship Some 3
Myelomeningocele co-occurrent with hydrocephalus (disorder) Associated morphology True Dilatation Inferred relationship Some 1
Idiopathic congenital megacolon Associated morphology False Dilatation Inferred relationship Some 1
Thoracic spina bifida with hydrocephalus - open Associated morphology True Dilatation Inferred relationship Some 5
Sacral spina bifida with hydrocephalus - open Associated morphology True Dilatation Inferred relationship Some 3
Thoracic spina bifida with hydrocephalus Associated morphology True Dilatation Inferred relationship Some 4
Spina bifida with hydrocephalus - closed Associated morphology True Dilatation Inferred relationship Some 3
Spina bifida with hydrocephalus - open Associated morphology True Dilatation Inferred relationship Some 4
Lumbar spina bifida with hydrocephalus - closed Associated morphology True Dilatation Inferred relationship Some 3
Sacral spina bifida with hydrocephalus - closed Associated morphology True Dilatation Inferred relationship Some 3

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