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719267003: Progressive cavitating leukoencephalopathy (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3315762017 Progressive cavitating leukoencephalopathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3315763010 Progressive cavitating leukoencephalopathy en Synonym Active Case insensitive SNOMED CT core
3789570016 Progressive cavitating leucoencephalopathy en Synonym Active Case insensitive SNOMED CT core
3315764016 Progressive cavitating leukoencephalopathy has characteristics of acute episodes of neurological deficit (ataxia, dysarthria, seizures) with irritability and opisthotonus followed by either steady deterioration or alternating periods of rapid progression and prolonged periods of stability. So far around 20 patients have been reported in the literature. Onset occurs in infancy or early childhood. The mode of transmission is autosomal recessive. en Definition Active Case sensitive SNOMED CT core
3789571017 Progressive cavitating leucoencephalopathy has characteristics of acute episodes of neurological deficit (ataxia, dysarthria, seizures) with irritability and opisthotonus followed by either steady deterioration or alternating periods of rapid progression and prolonged periods of stability. So far around 20 patients have been reported in the literature. Onset occurs in infancy or early childhood. The mode of transmission is autosomal recessive. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Progressive cavitating leukoencephalopathy Is a Leukoencephalopathy true Inferred relationship Some
Progressive cavitating leukoencephalopathy Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Progressive cavitating leukoencephalopathy Is a Hereditary disorder of nervous system true Inferred relationship Some
Progressive cavitating leukoencephalopathy Finding site Cerebral white matter structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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