FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

726702005: Epileptic encephalopathy with global cerebral demyelination (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3451871013 Epileptic encephalopathy with global cerebral demyelination (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3451872018 Epileptic encephalopathy with global cerebral demyelination en Synonym Active Entire term case insensitive SNOMED CT core module
3451873011 Mitochondrial aspartate-glutamate carrier 1 deficiency 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
Epileptic encephalopathy with global cerebral demyelination Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Epileptic encephalopathy with global cerebral demyelination Is a Anomalies of cerebrum false Inferred relationship Existential restriction modifier
Epileptic encephalopathy with global cerebral demyelination Is a Mitochondrial cytopathy true Inferred relationship Existential restriction modifier
Epileptic encephalopathy with global cerebral demyelination Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Epileptic encephalopathy with global cerebral demyelination Is a Epileptic encephalopathy true Inferred relationship Existential restriction modifier
Epileptic encephalopathy with global cerebral demyelination Has definitional manifestation Seizure false Inferred relationship Existential restriction modifier
Epileptic encephalopathy with global cerebral demyelination Associated morphology Hypomyelination false Inferred relationship Existential restriction modifier 2
Epileptic encephalopathy with global cerebral demyelination Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Epileptic encephalopathy with global cerebral demyelination Finding site Structure of cerebrum false Inferred relationship Existential restriction modifier 2
Epileptic encephalopathy with global cerebral demyelination Is a Congenital and developmental anomalies of the nervous system false Inferred relationship Existential restriction modifier
Epileptic encephalopathy with global cerebral demyelination Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Epileptic encephalopathy with global cerebral demyelination Associated morphology Hypomyelination true Inferred relationship Existential restriction modifier 1
Epileptic encephalopathy with global cerebral demyelination Finding site Structure of cerebrum true Inferred relationship Existential restriction modifier 1
Epileptic encephalopathy with global cerebral demyelination Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Epileptic encephalopathy with global cerebral demyelination Is a Congenital anomaly of cerebrum true Inferred relationship Existential restriction modifier
Epileptic encephalopathy with global cerebral demyelination Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start