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1373768001: Neuronal ceroid lipofuscinosis type 4 (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
5483354017 Neuronal ceroid lipofuscinosis type 4 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5483355016 Neuronal ceroid lipofuscinosis type 4 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5483356015 NCL4 - neuronal ceroid lipofuscinosis type 4 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5483357012 CLN4 disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5483358019 A rare neuronal ceroid lipofuscinosis characterized by adult-onset (20-early 30 years) progressive generalized tonic-clonic and myoclonic seizures, speech deterioration, dementia and ataxia. Some patients may also exhibit Parkinsonism. Visual impairment is usually not present. This is the only ceroid lipofuscinosis form inherited dominantly. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5483359010 A rare neuronal ceroid lipofuscinosis characterised by adult-onset (20-early 30 years) progressive generalised tonic-clonic and myoclonic seizures, speech deterioration, dementia and ataxia. Some patients may also exhibit Parkinsonism. Visual impairment is usually not present. This is the only ceroid lipofuscinosis form inherited dominantly. 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 4 Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Neuronal ceroid lipofuscinosis type 4 Is a Progressive myoclonic epilepsy true Inferred relationship Some
Neuronal ceroid lipofuscinosis type 4 Clinical course Progressive (qualifier value) true Inferred relationship Some 4
Neuronal ceroid lipofuscinosis type 4 Occurrence Congenital true Inferred relationship Some 3
Neuronal ceroid lipofuscinosis type 4 Occurrence Adulthood true Inferred relationship Some 1
Neuronal ceroid lipofuscinosis type 4 Finding site Brain structure true Inferred relationship Some 1
Neuronal ceroid lipofuscinosis type 4 Associated morphology Degenerative abnormality true Inferred relationship Some 1
Neuronal ceroid lipofuscinosis type 4 Is a Neuronal ceroid lipofuscinosis true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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