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1179293006: Erythrokeratodermia cardiomyopathy syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Oct 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4650575017 Erythrokeratodermia cardiomyopathy syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4650576016 Erythrokeratodermia cardiomyopathy syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4650577013 EKC (erythrokeratodermia cardiomyopathy) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Erythrokeratodermia cardiomyopathy syndrome Is a Hereditary disorder of tooth true Inferred relationship Existential restriction modifier
Erythrokeratodermia cardiomyopathy syndrome Is a Erythrokeratoderma true Inferred relationship Existential restriction modifier
Erythrokeratodermia cardiomyopathy syndrome Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier
Erythrokeratodermia cardiomyopathy syndrome Is a Congestive cardiomyopathy true Inferred relationship Existential restriction modifier
Erythrokeratodermia cardiomyopathy syndrome Is a Disorder of hard tissues of teeth true Inferred relationship Existential restriction modifier
Erythrokeratodermia cardiomyopathy syndrome Is a Disorder of skin true Inferred relationship Existential restriction modifier
Erythrokeratodermia cardiomyopathy syndrome Interprets Keratinization, function true Inferred relationship Existential restriction modifier 4
Erythrokeratodermia cardiomyopathy syndrome Has interpretation Abnormal true Inferred relationship Existential restriction modifier 4
Erythrokeratodermia cardiomyopathy syndrome Finding site Myocardium structure true Inferred relationship Existential restriction modifier 1
Erythrokeratodermia cardiomyopathy syndrome Associated morphology Dilatation true Inferred relationship Existential restriction modifier 1
Erythrokeratodermia cardiomyopathy syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 2
Erythrokeratodermia cardiomyopathy syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Erythrokeratodermia cardiomyopathy syndrome Finding site Enamel structure true Inferred relationship Existential restriction modifier 3
Erythrokeratodermia cardiomyopathy syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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