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1373774001: Neuronal ceroid lipofuscinosis type 7 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Oct 2025. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5483414018 Neuronal ceroid lipofuscinosis type 7 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5483415017 NCL7 - neuronal ceroid lipofuscinosis type 7 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5483416016 Neuronal ceroid lipofuscinosis type 7 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5483417013 A rare neuronal ceroid lipofuscinosis characterized by epilepsy with myoclonic, atonic, and bilateral tonic-clonic seizures, gait disturbance, and language difficulty/delay. Progressive motor and cognitive decline, personality disorders, myoclonus and visual loss are common clinical features become evident later in the disease progress. Age of onset is typically late-infantile, however few juvenile-onset patients are reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5483418015 A rare neuronal ceroid lipofuscinosis characterised by epilepsy with myoclonic, atonic, and bilateral tonic-clonic seizures, gait disturbance, and language difficulty/delay. Progressive motor and cognitive decline, personality disorders, myoclonus and visual loss are common clinical features become evident later in the disease progress. Age of onset is typically late-infantile, however few juvenile-onset patients are reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neuronal ceroid lipofuscinosis type 7 Is a Progressive myoclonic epilepsy true Inferred relationship Some
Neuronal ceroid lipofuscinosis type 7 Is a Neuronal ceroid lipofuscinosis true Inferred relationship Some
Neuronal ceroid lipofuscinosis type 7 Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Neuronal ceroid lipofuscinosis type 7 Clinical course Progressive (qualifier value) true Inferred relationship Some 3
Neuronal ceroid lipofuscinosis type 7 Occurrence Congenital true Inferred relationship Some 2
Neuronal ceroid lipofuscinosis type 7 Finding site Brain structure true Inferred relationship Some 1
Neuronal ceroid lipofuscinosis type 7 Associated morphology Degenerative abnormality true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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