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784377008: Autosomal dominant epilepsy with auditory features (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3763852010 Partial epilepsy with auditory aura en Synonym Active Entire term case insensitive SNOMED CT core module
3763853017 Autosomal dominant epilepsy with auditory features (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3763854011 Autosomal dominant epilepsy with auditory features en Synonym Active Entire term case insensitive SNOMED CT core module
3763855012 Autosomal dominant lateral temporal lobe epilepsy en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant epilepsy with auditory features Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant epilepsy with auditory features Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Autosomal dominant epilepsy with auditory features Is a Familial disease true Inferred relationship Existential restriction modifier
Autosomal dominant epilepsy with auditory features Is a Temporal lobe epilepsy true Inferred relationship Existential restriction modifier
Autosomal dominant epilepsy with auditory features Finding site Temporal lobe structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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