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58258004: Infantile neuronal ceroid lipofuscinosis (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1231818019 Hagberg-Santavouri type neuronal ceroid lipofuscinosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1231819010 Neuronal ceroid lipofuscinosis infantile Finnish type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1231820016 Polyunsaturated fatty acid lipidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1231821017 Haltia-Santavouri type neuronal ceroid lipofuscinosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
445521000241111 céroïde-lipofuscinose neuronale infantile (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
796970016 Infantile neuronal ceroid lipofuscinosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
893111000172116 céroïde-lipofuscinose neuronale infantile fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
952631000172114 CLN (céroïde-lipofuscinose neuronale) infantile fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
96816010 Infantile neuronal ceroid lipofuscinosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
96817018 Hagberg-Santavuori disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
96818011 Santavuori disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
96819015 Neuronal ceroid lipofuscinosis, infantile Finnish type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
96820014 Polyunsaturated acid lipidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
céroïde-lipofuscinose neuronale infantile (trouble) morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
céroïde-lipofuscinose neuronale infantile (trouble) est un(e) (attribut) céroïde-lipofuscinose neuronale true Inferred relationship Some
céroïde-lipofuscinose neuronale infantile (trouble) survenue (attribut) congénital true Inferred relationship Some 2
céroïde-lipofuscinose neuronale infantile (trouble) morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some
céroïde-lipofuscinose neuronale infantile (trouble) morphologie associée (attribut) dégénérescence false Inferred relationship Some 1
céroïde-lipofuscinose neuronale infantile (trouble) localisation d'une constatation (attribut) système nerveux true Inferred relationship Some 3
Inbound Relationships Type Active Source Characteristic Refinability Group
Progressive myoclonic epilepsy type 3 est un(e) (attribut) True céroïde-lipofuscinose neuronale infantile (trouble) Inferred relationship Some
Late-infantile neuronal ceroid lipofuscinosis est un(e) (attribut) True céroïde-lipofuscinose neuronale infantile (trouble) Inferred relationship Some

This concept is not in any reference sets

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