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43916004: Mucopolysaccharidosis type VII (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2971858017 Mucopolysaccharidosis type VII (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
493710017 Sly disease en Synonym Active Case sensitive SNOMED CT core
493711018 Mucopolysaccharidosis type VII en Synonym Active Initial character case insensitive SNOMED CT core
493712013 Beta-glucuronidase deficiency en Synonym Active Case insensitive SNOMED CT core
493713015 MPS VII - Mucopolysaccharidosis VII en Synonym Active Case sensitive SNOMED CT core
73228011 Mucopolysaccharidosis, MPS-VII en Synonym Active Initial character case insensitive SNOMED CT core
73229015 Sly syndrome en Synonym Active Case sensitive SNOMED CT core
73230013 beta-Glucuronidase deficiency en Synonym Active Case sensitive SNOMED CT core
73231012 GUSB deficiency en Synonym Active Case sensitive SNOMED CT core
73232017 GUS deficiency en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mucopolysaccharidosis, MPS-VII Is a Mucopolysaccharidosis true Inferred relationship Some
Mucopolysaccharidosis, MPS-VII Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Mucopolysaccharidosis, MPS-VII Occurrence Congenital true Inferred relationship Some 1
Mucopolysaccharidosis, MPS-VII Finding site Body system structure false Inferred relationship Some

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

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