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

189979005: Globoid cell leukodystrophy, early onset (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2668834014 Globoid cell leukodystrophy, early onset en Synonym Active Case insensitive SNOMED CT core
291916011 Galactosylceramide lipidosis en Synonym Active Case insensitive SNOMED CT core
291917019 Familial infantile diffuse brain sclerosis en Synonym Active Case insensitive SNOMED CT core
291918012 Diffuse globoid body sclerosis en Synonym Active Case insensitive SNOMED CT core
573498013 Globoid cell leukodystrophy, early onset (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Galactosylceramide lipidosis Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Galactosylceramide lipidosis Due to Galactocerebroside beta-galactosidase deficiency - early onset true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Back to Start