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472316006: Hypertrophic mitochondrial cardiomyopathy (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2951109019 Hypertrophic mitochondrial cardiomyopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2951132015 Hypertrophic mitochondrial cardiomyopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

10 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypertrophic mitochondrial cardiomyopathy (disorder) est un(e) (attribut) Hypertrophic cardiomyopathy due to disorder true Inferred relationship Some
Hypertrophic mitochondrial cardiomyopathy (disorder) est un(e) (attribut) cardiomyopathie hypertrophique false Inferred relationship Some
Hypertrophic mitochondrial cardiomyopathy (disorder) est un(e) (attribut) Mitochondrial cardiomyopathy (disorder) true Inferred relationship Some
Hypertrophic mitochondrial cardiomyopathy (disorder) Due to Mitochondrial cytopathy true Inferred relationship Some 1
Hypertrophic mitochondrial cardiomyopathy (disorder) morphologie associée (attribut) hypertrophie true Inferred relationship Some 2
Hypertrophic mitochondrial cardiomyopathy (disorder) localisation d'une constatation (attribut) structure du myocarde true Inferred relationship Some 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency (disorder) est un(e) (attribut) True Hypertrophic mitochondrial cardiomyopathy (disorder) Inferred relationship Some
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial deoxyribonucleic acid mutation (disorder) est un(e) (attribut) True Hypertrophic mitochondrial cardiomyopathy (disorder) Inferred relationship Some
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency est un(e) (attribut) True Hypertrophic mitochondrial cardiomyopathy (disorder) Inferred relationship Some
Combined oxidative phosphorylation defect type 17 (disorder) est un(e) (attribut) True Hypertrophic mitochondrial cardiomyopathy (disorder) Inferred relationship Some
Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome est un(e) (attribut) True Hypertrophic mitochondrial cardiomyopathy (disorder) Inferred relationship Some
Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome (disorder) est un(e) (attribut) True Hypertrophic mitochondrial cardiomyopathy (disorder) Inferred relationship Some
QRSL1-related combined oxidative phosphorylation defect est un(e) (attribut) True Hypertrophic mitochondrial cardiomyopathy (disorder) Inferred relationship Some
Hypertrophic mitochondrial cardiomyopathy associated with cataracts and lactic acidosis (disorder) est un(e) (attribut) True Hypertrophic mitochondrial cardiomyopathy (disorder) Inferred relationship Some
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) est un(e) (attribut) True Hypertrophic mitochondrial cardiomyopathy (disorder) Inferred relationship Some
Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome (disorder) est un(e) (attribut) True Hypertrophic mitochondrial cardiomyopathy (disorder) Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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