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

233873004: Hypertrophic cardiomyopathy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
350415017 Hypertrophic cardiomyopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
350416016 HCM - Hypertrophic cardiomyopathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
622117015 Hypertrophic cardiomyopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1845461000195113 cardiomiopatia ipertrofica it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
306781000077113 cardiomyopathie hypertrophique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
393881000274111 Hypertrophe Kardiomyopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


34 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypertrophic cardiomyopathy Is a Cardiomyopathy true Inferred relationship Some
Hypertrophic cardiomyopathy Finding site Structure of outflow tract of left ventricle false Inferred relationship Some 1
Hypertrophic cardiomyopathy Finding site Myocardium structure false Inferred relationship Some
Hypertrophic cardiomyopathy Associated morphology Hypertrophy false Inferred relationship Some 1
Hypertrophic cardiomyopathy Is a Ventricular hypertrophy false Inferred relationship Some
Hypertrophic cardiomyopathy Is a Left ventricular hypertrophy false Inferred relationship Some
Hypertrophic cardiomyopathy Associated morphology Hypertrophy false Inferred relationship Some 1
Hypertrophic cardiomyopathy Finding site Structure of outflow tract of left ventricle false Inferred relationship Some 1
Hypertrophic cardiomyopathy Finding site Structure of myocardium of left ventricle false Inferred relationship Some 1
Hypertrophic cardiomyopathy Associated morphology Hypertrophy false Inferred relationship Some 1
Hypertrophic cardiomyopathy Finding site Structure of myocardium of left ventricle false Inferred relationship Some 1
Hypertrophic cardiomyopathy Associated morphology Hypertrophy true Inferred relationship Some 2
Hypertrophic cardiomyopathy Is a Structural disorder of heart (disorder) true Inferred relationship Some
Hypertrophic cardiomyopathy Finding site Myocardium structure true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Hypertrophic cardiomyopathy without obstruction Is a True Hypertrophic cardiomyopathy Inferred relationship Some
Hypertrophic obstructive cardiomyopathy Is a True Hypertrophic cardiomyopathy Inferred relationship Some
Hypertrophic cardiomyopathy secondary to Friedreich's ataxia Is a False Hypertrophic cardiomyopathy Inferred relationship Some
Canine hypertrophic cardiomyopathy Is a False Hypertrophic cardiomyopathy Inferred relationship Some
Hypertrophic cardiomyopathy secondary to hyperthyroidism Is a False Hypertrophic cardiomyopathy Inferred relationship Some
[X]Other hypertrophic cardiomyopathy Is a False Hypertrophic cardiomyopathy Inferred relationship Some
Hypertrophic cardiomyopathy secondary to neuromuscular disorder Is a False Hypertrophic cardiomyopathy Inferred relationship Some
Primary familial hypertrophic cardiomyopathy Is a False Hypertrophic cardiomyopathy Inferred relationship Some
Feline hypertrophic cardiomyopathy Is a False Hypertrophic cardiomyopathy Inferred relationship Some
Hypertrophic cardiomyopathy associated with another disorder Is a False Hypertrophic cardiomyopathy Inferred relationship Some
Hypertrophic cardiomyopathy with genetic marker (disorder) Is a True Hypertrophic cardiomyopathy Inferred relationship Some
Hypertrophic mitochondrial cardiomyopathy (disorder) Is a False Hypertrophic cardiomyopathy Inferred relationship Some
Fetal hypertrophic cardiomyopathy (disorder) Is a True Hypertrophic cardiomyopathy Inferred relationship Some
Primary hypertrophic cardiomyopathy (disorder) Is a True Hypertrophic cardiomyopathy Inferred relationship Some
Cardiac septal myectomy (procedure) Has focus True Hypertrophic cardiomyopathy Inferred relationship Some 1
A rare disorder characterized by progressive, late onset, autosomal dominant sensorineural hearing loss, QT interval prolongation, and mild cardiac hypertrophy. Is a True Hypertrophic cardiomyopathy Inferred relationship Some
Cardiomyopathy and renal anomaly syndrome (disorder) Is a True Hypertrophic cardiomyopathy Inferred relationship Some
A rare mitochondrial disease that has a heterogeneous clinical presentation characterized by the association of progressive sensorineural hearing loss with hypertrophic cardiomyopathy and, in the majority of cases, encephalomyopathy symptoms such as ataxia, slurred speech, progressive external ophthalmoparesis (PEO), muscle weakness, myalgia, and exercise intolerance. Is a True Hypertrophic cardiomyopathy Inferred relationship Some
Glycogen storage disease due to muscle and heart glycogen synthase deficiency is characterized by muscle and heart glycogen deficiency. It has been described in three siblings (two brothers and their younger sister). The older brother died at 10.5 years of age as a result of sudden cardiac arrest and the younger brother presented with hypertrophic cardiomyopathy, abnormal heart rate and blood pressure during exercise, and muscle fatigability. The sister showed no symptoms but a lack of glycogen was identified through muscle biopsy. The syndrome is caused by homozygous missense mutations in the gene encoding muscle glycogen synthase. Is a False Hypertrophic cardiomyopathy Inferred relationship Some
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome is a rare mitochondrial disease due to a defect in coenzyme Q10 biosynthesis that manifests with a broad spectrum of signs and symptoms which may include: neonatal lactic acidosis, global developmental delay, tonus disorder, seizures, reduced spontaneous movements, ventricular hypertrophy, bradycardia, renal tubular dysfunction with massive lactic acid excretion in urine, severe biochemical defect of respiratory chain complexes II/III when assayed together and deficiency of coenzyme Q10 in skeletal muscle. Cerebral and cerebellar atrophy can be seen on magnetic resonance imaging and multiple choroid plexus cysts and symmetrical hyperechoic signal alterations in basal ganglia have been observed on ultrasound. Is a False Hypertrophic cardiomyopathy Inferred relationship Some
Hypertrophic cardiomyopathy due to glycogen storage disease Is a False Hypertrophic cardiomyopathy Inferred relationship Some
Hypertrophic cardiomyopathy due to lysosomal disease Is a False Hypertrophic cardiomyopathy Inferred relationship Some
Hypertrophy of septomarginal trabeculation (disorder) Is a True Hypertrophic cardiomyopathy Inferred relationship Some
Hypertrophic cardiomyopathy due to disorder Is a True Hypertrophic cardiomyopathy Inferred relationship Some
Apical hypertrophic cardiomyopathy Is a True Hypertrophic cardiomyopathy Inferred relationship Some

This concept is not in any reference sets

Back to Start