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783064000: Progressive myoclonic epilepsy type 3 (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
3757310011 Progressive myoclonic epilepsy due to KCTD7 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
3757311010 Progressive myoclonus epilepsy type 3 en Synonym Active Entire term case insensitive SNOMED CT core module
3757312015 PME type 3 - progressive myoclonic epilepsy type 3 en Synonym Active Entire term case sensitive SNOMED CT core module
3757313013 Progressive myoclonic epilepsy type 3 en Synonym Active Entire term case insensitive SNOMED CT core module
3757314019 Progressive myoclonic epilepsy type 3 (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
Progressive myoclonic epilepsy type 3 Is a Infantile neuronal ceroid lipofuscinosis true Inferred relationship Existential restriction modifier
Progressive myoclonic epilepsy type 3 Is a Chronic brain syndrome true Inferred relationship Existential restriction modifier
Progressive myoclonic epilepsy type 3 Is a Cerebral degeneration true Inferred relationship Existential restriction modifier
Progressive myoclonic epilepsy type 3 Finding site Structure of cerebrum true Inferred relationship Existential restriction modifier 1
Progressive myoclonic epilepsy type 3 Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Progressive myoclonic epilepsy type 3 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 1
Progressive myoclonic epilepsy type 3 Is a Progressive myoclonic epilepsy true Inferred relationship Existential restriction modifier
Progressive myoclonic epilepsy type 3 Is a Chronic metabolic disorder true Inferred relationship Existential restriction modifier
Progressive myoclonic epilepsy type 3 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Progressive myoclonic epilepsy type 3 Clinical course Progressive true Inferred relationship Existential restriction modifier 2
Progressive myoclonic epilepsy type 3 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Progressive myoclonic epilepsy type 3 Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
Progressive myoclonic epilepsy type 3 Interprets Movement false 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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