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900000000000527005: SAME AS association reference set (foundation metadata concept)


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

Descriptions:

Id Description Lang Type Status Case? Module
900000000001158011 SAME AS association reference set (foundation metadata concept) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)
900000000001159015 SAME AS association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)


43627 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
SAME AS association reference set (foundation metadata concept) Is a Historical association reference set (foundation metadata concept) true Inferred relationship Some

Members targetComponentId
ssDNA binding autoantibody level Antibody to single stranded DNA measurement
ssDNA binding autoantibody level Antibody to single stranded DNA measurement
tRNA cytidylyltransferase tRNA adenylyltransferase
tRNA nucleotidyltransferase tRNA adenylyltransferase
u/kg ug/kg
van der Hoeves syndrom Osteogenesis imperfecta type I (disorder)
von Frey's syndrome Auriculotemporal syndrome
von Willebrands sjukdom, typ 2N Hereditary von Willebrand disease type 2N (disorder)
von Willebrands sjukdom, typ 2A Hereditary von Willebrand disease type 2A
von Willebrand disease type 2A Hereditary von Willebrand disease type 2A
von Willebrands sjukdom, typ 2B Hereditary von Willebrand disease type 2B
von Willebrand disease type 2B Hereditary von Willebrand disease type 2B
von Willebrands sjukdom, typ 2M Hereditary von Willebrand disease type 2M
von Willebrand disease type 2M Hereditary von Willebrand disease type 2M
von Willebrand disease type 2N Hereditary von Willebrand disease type 2N (disorder)
von Willebrand disease type IA Hereditary von Willebrand disease type 1A
von Willebrands sjukdom, typ 1A Hereditary von Willebrand disease type 1A
von Willebrands sjukdom, typ 2A Hereditary von Willebrand disease type 2A
von Willebrands sjukdom, typ 2B Hereditary von Willebrand disease type 2B
von Willebrand factor activity Von Willebrand factor activity measurement (procedure)
von Willebrand factor activity Von Willebrand factor activity measurement (procedure)
von Willebrand factor antigen von Willebrand factor antigen
von Willebrand factor level Factor VIII R: WF assay
von Willebrand factor level Factor VIII R: WF assay
von Willebrand factor multimeric analysis von Willebrand factor multimer assay
von Willebrand factor ristocetin cofactor von Willebrand factor
von Willebrand's disease von Willebrand disorder

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