FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

230410004: Benign neonatal familial convulsions (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
345270013 Benign neonatal epilepsy en Synonym Active Entire term case insensitive SNOMED CT core module
345271012 BFNC - Benign familial neonatal convulsions en Synonym Active Entire term case sensitive SNOMED CT core module
345272017 Benign neonatal familial convulsions en Synonym Active Entire term case insensitive SNOMED CT core module
618214010 Benign neonatal familial convulsions (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Benign neonatal familial convulsions Is a Idiopathic generalized epilepsy false Inferred relationship Existential restriction modifier
Benign neonatal familial convulsions Is a Benign neonatal convulsions true Inferred relationship Existential restriction modifier
Benign neonatal familial convulsions Occurrence Neonatal true Inferred relationship Existential restriction modifier 1
Benign neonatal familial convulsions Finding site Structure of cerebrum false Inferred relationship Existential restriction modifier 2
Benign neonatal familial convulsions Occurrence Perinatal state false Inferred relationship Existential restriction modifier
Benign neonatal familial convulsions Occurrence Perinatal period false Inferred relationship Existential restriction modifier
Benign neonatal familial convulsions Has definitional manifestation Seizure false Inferred relationship Existential restriction modifier
Benign neonatal familial convulsions Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Benign neonatal familial convulsions Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Benign neonatal familial convulsions 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

Back to Start