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733082001: Early-onset Lafora body disease (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
3498694013 Early-onset Lafora body disease (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3498695014 Early-onset Lafora body disease en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Early-onset Lafora body disease Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Early-onset Lafora body disease Is a Progressive myoclonic epilepsy true Inferred relationship Existential restriction modifier
Early-onset Lafora body disease Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Early-onset Lafora body disease Has definitional manifestation Seizure false Inferred relationship Existential restriction modifier
Early-onset Lafora body disease Associated morphology Lafora body true Inferred relationship Existential restriction modifier 2
Early-onset Lafora body disease Occurrence Childhood true Inferred relationship Existential restriction modifier 2
Early-onset Lafora body disease Finding site Structure of cerebrum true Inferred relationship Existential restriction modifier 2
Early-onset Lafora body disease Is a Childhood seizure false Inferred relationship Existential restriction modifier
Early-onset Lafora body disease Interprets Movement false 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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