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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
350415017 Hypertrophic cardiomyopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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
350417013 Primary hypertrophic cardiomyopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
622117015 Hypertrophic cardiomyopathy (disorder) en Fully specified name Active Only initial character case insensitive (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
393881000274111 Hypertrophe Kardiomyopathie de 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
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 (disorder) Is a Cardiomyopathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic cardiomyopathy (disorder) Finding site Structure of outflow tract of left ventricle false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertrophic cardiomyopathy (disorder) Finding site Myocardium structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic cardiomyopathy (disorder) Associated morphology Hypertrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertrophic cardiomyopathy (disorder) Is a Ventricular hypertrophy false Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic cardiomyopathy (disorder) Is a Left ventricular hypertrophy false Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic cardiomyopathy (disorder) Associated morphology Hypertrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertrophic cardiomyopathy (disorder) Finding site Structure of outflow tract of left ventricle false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertrophic cardiomyopathy (disorder) Finding site Structure of myocardium of left ventricle false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertrophic cardiomyopathy (disorder) Associated morphology Hypertrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertrophic cardiomyopathy (disorder) Finding site Structure of myocardium of left ventricle false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypertrophic cardiomyopathy (disorder) Associated morphology Hypertrophy true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypertrophic cardiomyopathy (disorder) Is a Structural disorder of heart true Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic cardiomyopathy (disorder) Finding site Myocardium structure true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Hypertrophic cardiomyopathy without obstruction Is a True Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic obstructive cardiomyopathy Is a True Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic cardiomyopathy secondary to Friedreich's ataxia Is a False Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Canine hypertrophic cardiomyopathy Is a False Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic cardiomyopathy secondary to hyperthyroidism Is a False Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
[X]Other hypertrophic cardiomyopathy Is a False Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic cardiomyopathy secondary to neuromuscular disorder Is a False Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Primary familial hypertrophic cardiomyopathy (disorder) Is a False Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Feline hypertrophic cardiomyopathy Is a False Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic cardiomyopathy associated with another disorder Is a False Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic cardiomyopathy with genetic marker (disorder) Is a True Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic mitochondrial cardiomyopathy (disorder) Is a False Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Fetal hypertrophic cardiomyopathy (disorder) Is a True Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Primary hypertrophic cardiomyopathy (disorder) Is a True Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cardiac septal myectomy (procedure) Has focus True Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 1
Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome Is a True Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cardiomyopathy and renal anomaly syndrome (disorder) Is a True Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Maternally inherited cardiomyopathy and hearing loss syndrome (disorder) Is a True Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
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 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome Is a False Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic cardiomyopathy due to glycogen storage disease Is a False Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic cardiomyopathy due to lysosomal disease (disorder) Is a False Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophy of septomarginal trabeculation (disorder) Is a True Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic cardiomyopathy due to disorder Is a True Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Apical hypertrophic cardiomyopathy Is a True Hypertrophic cardiomyopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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