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1237571004: Benign familial infantile epilepsy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5099849014 Benign familial infantile epilepsy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5099850014 BFIE - benign familial infantile epilepsy en Synonym Active Entire term case sensitive SNOMED CT core module
5099851013 BFIS - benign familial infantile seizures en Synonym Active Entire term case sensitive SNOMED CT core module
5099852018 Benign familial infantile epilepsy en Synonym Active Entire term case insensitive SNOMED CT core module
5099853011 Benign familial infantile convulsions 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
Benign familial infantile epilepsy Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Benign familial infantile epilepsy Is a Partial seizure true Inferred relationship Existential restriction modifier
Benign familial infantile epilepsy Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Benign familial infantile epilepsy Is a Epilepsy true Inferred relationship Existential restriction modifier
Benign familial infantile epilepsy Occurrence Infancy true Inferred relationship Existential restriction modifier 1
Benign familial infantile epilepsy Finding site Structure of cerebrum 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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