FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

238028008: Sphingolipidosis (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
356771012 Sphingolipidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
549591000241117 sphingolipidose (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
626850015 Sphingolipidosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
905151000172111 sphingolipidose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


32 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Sphingolipidosis localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Sphingolipidosis survenue (attribut) congénital false Inferred relationship Some
Sphingolipidosis est un(e) (attribut) Disorder of lipid storage and metabolism true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Fabry's disease est un(e) (attribut) True Sphingolipidosis Inferred relationship Some
Gaucher's disease est un(e) (attribut) True Sphingolipidosis Inferred relationship Some
Galactosylceramide beta-galactosidase deficiency est un(e) (attribut) True Sphingolipidosis Inferred relationship Some
Metachromatic leukodystrophy est un(e) (attribut) False Sphingolipidosis Inferred relationship Some
Globoid cell leucodystrophy, late-onset est un(e) (attribut) False Sphingolipidosis Inferred relationship Some
Metachromatic leucodystrophy (disorder) est un(e) (attribut) True Sphingolipidosis Inferred relationship Some
déficit multiple en sulfatases (trouble) est un(e) (attribut) True Sphingolipidosis Inferred relationship Some
Sphingomyelin/cholesterol lipidosis (disorder) est un(e) (attribut) True Sphingolipidosis Inferred relationship Some
Galactocerebroside beta-galactosidase deficiency - early onset est un(e) (attribut) False Sphingolipidosis Inferred relationship Some
Encephalopathy due to prosaposin deficiency (disorder) est un(e) (attribut) True Sphingolipidosis Inferred relationship Some
Autosomal recessive cerebellar ataxia with late-onset spasticity est un(e) (attribut) True Sphingolipidosis Inferred relationship Some

This concept is not in any reference sets

Back to Start