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1296784002: Neuronal ceroid lipofuscinosis type 6A (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Dec 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5287022018 CLN6-related neuronal ceroid lipofuscinosis type 6A en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5287024017 Neuronal ceroid lipofuscinosis type 6A (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5287025016 CLN6 transmembrane ER protein-related neuronal ceroid lipofuscinosis type 6A en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5287298016 Neuronal ceroid lipofuscinosis type 6A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5287299012 vLINCL - variant late infantile neuronal ceroid lipofuscinosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5488332016 Late infantile CLN6 disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5488333014 Late infantile neuronal ceroid lipofuscinosis type 6 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5287028019 An autosomal recessive neurodegenerative disorder with a variable age at onset in the first years of life after normal early development followed by decline of mental and motor capacities, epilepsy, and vision loss through retinal degeneration. Caused by homozygous or compound heterozygous mutation in the CLN6 gene on chromosome 15q23. 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 6A (disorder) Occurrence Congenital true Inferred relationship Some 2
Neuronal ceroid lipofuscinosis type 6A (disorder) Finding site Structure of nervous system (body structure) false Inferred relationship Some 1
Neuronal ceroid lipofuscinosis type 6A (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 1
Neuronal ceroid lipofuscinosis type 6A (disorder) Is a Infantile neuronal ceroid lipofuscinosis (disorder) false Inferred relationship Some
Neuronal ceroid lipofuscinosis type 6A (disorder) Is a Autosomal recessive hereditary disorder false Inferred relationship Some
Neuronal ceroid lipofuscinosis type 6A (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 4
Neuronal ceroid lipofuscinosis type 6A (disorder) Finding site Brain structure true Inferred relationship Some 1
Neuronal ceroid lipofuscinosis type 6A (disorder) Is a Neuronal ceroid lipofuscinosis type 6 (disorder) true Inferred relationship Some
Neuronal ceroid lipofuscinosis type 6A (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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