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87074006: Salla disease (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
1235196011 Adult sialic acid storage disease en Synonym Active Case insensitive SNOMED CT core
144398018 Salla disease en Synonym Active Case sensitive SNOMED CT core
144399014 Sialuria, Finnish type en Synonym Active Initial character case insensitive SNOMED CT core
829471018 Salla disease (disorder) en Fully specified name Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Salla disease Pathological process Pathological developmental process true Inferred relationship Some 1
Salla disease Occurrence Congenital true Inferred relationship Some 1
Salla disease Associated morphology Congenital dysplasia false Inferred relationship Some 1
Salla disease Is a Sialic storage disease true Inferred relationship Some
Salla disease Is a Lipid storage disease true Inferred relationship Some
Salla disease Associated morphology Congenital dysplasia false Inferred relationship Some 1
Salla disease Finding site Bone structure false Inferred relationship Some 1
Salla disease Occurrence Congenital false Inferred relationship Some 2
Salla disease Finding site Bone structure false Inferred relationship Some 2
Salla disease Associated morphology Congenital dysplasia false Inferred relationship Some 2
Salla disease Associated morphology Dysplasia true Inferred relationship Some 1
Salla disease Finding site Skeletal system structure false Inferred relationship Some 1
Salla disease Finding site Bone structure true Inferred relationship Some 1
Salla disease Occurrence Congenital false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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