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

SNOMED CT Concept\SNOMED CT Model Component\Foundation metadata concept (foundation metadata concept)\Reference set\Association type\Historical association reference set (foundation metadata concept)\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)

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
[Glycogen-synthase-D]-phosphatase	Glycogen-synthase-D phosphatase
[M]Acute monocytic leukaemia	Acute monocytic leukaemia
[M]Choroid plexus papilloma NOS	Benign choroid plexus papilloma (morphologic abnormality)
[M]Chronic erythraemia	Polycythemia vera
[M]Chronic lymphoid leukaemia	B-cell chronic lymphocytic leukemia/small lymphocytic lymphoma
[M]Chronic monocytic leukaemia	Chronic myelomonocytic leukemia
[M]Dermoid cyst	Teratoma, benign
[M]Eccrine dermal cylindroma	Eccrine dermal cylindroma
[M]Extra-adrenal paraganglioma, NOS	Extra-adrenal paraganglioma
[M]Glioma NOS	Glioma, malignant (morphologic abnormality)
[M]Gliomas	Glioma
[M]Leukaemic reticuloendotheliosis	Hairy cell leukemia
[M]Megakaryocytic leukaemia	Acute megakaryoblastic leukemia
[M]Mycosis fungoides	Mycosis fungoides
[M]Subependymal astrocytoma NOS	Subependymal glioma
[M]Waldenstrom's macroglobulinaemia	Waldenstrom's macroglobulinemia
[Myelin basic protein]-arginine N-methyltransferase	Histone-arginine N-methyltransferase (substance)
[Pyruvate dehydrogenase (lipoamide)]-phosphatase	Pyruvate dehydrogenase lipoamide-phosphatase
acute myocardial infarction of posterolateral wall (disorder)	Acute myocardial infarction of posterolateral wall
alpha Chloralose	Alphachloralose
alpha-Amylase (substance)	Alpha-amylase (substance)
préparation d'alpha-amylase	Alpha-amylase (substance)
alpha-Glucosidase (substance)	Alpha-glucosidase (substance)
alpha-Lactalbumin (substance)	Alpha-lactalbumin (substance)
alpha-N-Acetylgalactosaminidase	N-Acetyl-alpha-galactosaminidase
alpha>1< Antichymotrypsin	Alpha-1-antichymotrypsin
alpha>1< Glycoprotein	Alpha-1- acid glycoprotein (substance)
alpha>2< Antiplasmin	Antiplasmin
alpha>2< Globulin	Alpha 2 globulin
beta Carotene preparation	Product containing betacarotene (medicinal product)
beta-Amylase (substance)	Beta-amylase (substance)
beta-Hydroxybutyrate	3-hydroxybutyrate
day	day
syndrome de De Barsy	De Barsy syndrome (DBS) is characterized by facial dysmorphism (down-slanting palpebral fissures, a broad flat nasal bridge and a small mouth) with a progeroid appearance, large and late-closing fontanel, cutis laxa (CL), joint hyperlaxity, athetoid movements and hyperreflexia, pre- and postnatal growth retardation, intellectual deficit and developmental delay, and corneal clouding and cataract.
degrees of arc	degrees of arc
delta Aminolevulinic acid	5-aminolevulinic acid (substance)
delta-Aminolevulinic acid	5-aminolevulinic acid (substance)
dsDNA binding autoantibody level	Antibody to double stranded DNA measurement
dsDNA binding autoantibody level	Antibody to double stranded DNA measurement
Pteroyl-poly-alpha-glutamate hydrolase	Gamma-glutamyl hydrolase (substance)
gamma-Hydroxybutyrate	4-hydroxybutyrate
mL/s	mL/s
mmol/g dry weight tissue	mmol/g dry weight tissue
n-Acetyl glucosamine	N-Acetylglucosamine
n-Butylglycidylether	N-butyl glycidyl ether
n-Caproic acid	Caproic acid
n-Hexane	Hexane
n-Hexane measurement	Hexane measurement
n-Methyl-3, 4-methylenedioxyamphetamine	Methylenedioxymethamphetamine (substance)
n-Pentane	Pentane
n-Propyl alcohol	Propanol
n-Valeric acid	Valeric acid (substance)
o-Phenylphenol	2-phenylphenol
oz	oz
oz	oz
p-29 antibody	Antiproteinase 3 antibody
p-Chlorometacresol	Chlorocresol
p-Nitrophenol	Para-nitrophenol
p-tert-Butylphenol	p-tert-butylphenol (substance)
pM category	pM category (observable entity)
pN category	pN category (observable entity)
pT category	pT category (observable entity)
r' phenotype	cde haplotype (finding)
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
syndrome de van der Hoeve et de Kleyn	Osteogenesis imperfecta type I (disorder)
von Frey's syndrome	Auriculotemporal syndrome
von Willebrand disease Normandy	Hereditary von Willebrand disease type 2N (disorder)
von Willebrand disease type 2A	Hereditary von Willebrand disease type 2A
maladie de von Willebrand type 2A	Hereditary von Willebrand disease type 2A
von Willebrand disease type 2B	Hereditary von Willebrand disease type 2B
maladie de von Willebrand type 2B	Hereditary von Willebrand disease type 2B
von Willebrand disease type 2M	Hereditary von Willebrand disease type 2M
maladie de von Willebrand 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 Willebrand disease type IA	Hereditary von Willebrand disease type 1A
von Willebrand disease, type IIA	Hereditary von Willebrand disease type 2A
von Willebrand disease, type IIB	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 (substance)
von Willebrand's disease	Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome.

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Reference Sets

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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)