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1220598005: Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy (disorder)


Status: current, Primitive. Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5045351013 Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
5045355016 Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy en Synonym Active Case insensitive SNOMED CT core
5045356015 Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy en Synonym Active Case insensitive SNOMED CT core
5045353011 A rare mitochondrial disease with characteristics of a distinctive MRI pattern of cavitating leukodystrophy, predominantly in the posterior region of the cerebral hemispheres. The clinical picture varies widely between acute neurometabolic decompensation in infancy with loss of developmental milestones, seizures and pyramidal signs rapidly evolving into spastic tetraparesis, to subtle neurological symptoms presenting in adolescence. The disease course tends to stabilize over time in most patients and marked recovery of milestones may be observed. en Definition Active Case sensitive SNOMED CT core
5045354017 A rare mitochondrial disease with characteristics of a distinctive MRI pattern of cavitating leucodystrophy, predominantly in the posterior region of the cerebral hemispheres. The clinical picture varies widely between acute neurometabolic decompensation in infancy with loss of developmental milestones, seizures and pyramidal signs rapidly evolving into spastic tetraparesis, to subtle neurological symptoms presenting in adolescence. The disease course tends to stabilise over time in most patients and marked recovery of milestones may be observed. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy Is a Hereditary degenerative disease of central nervous system true Inferred relationship Some
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy Is a Leucodystrophy true Inferred relationship Some
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy Is a Mitochondrial cytopathy true Inferred relationship Some
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy Is a Peripheral neuropathy true Inferred relationship Some
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy Clinical course Non-progressive true Inferred relationship Some 3
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy Finding site Peripheral nerve structure true Inferred relationship Some 4
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy Finding site Myelinated nerve fibre structure true Inferred relationship Some 1
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy Associated morphology Myelin sheath alteration true Inferred relationship Some 1
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy Finding site White matter structure of brain and spinal cord true Inferred relationship Some 2
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy Associated morphology Dystrophy true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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