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
Decreased hemoglobin	Hemoglobin below reference range (finding)
Decreased serum protein level	Serum proteins below reference range
Decreased stability of joint	Instability of joint (finding)
Dedifferentiated liposarcoma	Dedifferentiated liposarcoma
Deep S wave	Deep S wave
Deep X-ray therapy 150-400 kV	Deep X-ray therapy 150-400 kV
Deep bruising	Deep contusion
Deep fibromatosis	A desmoid tumor (DT) is a benign, locally invasive soft tissue tumor associated with a high recurrence rate but with no metastatic potential.
Deep keratitis	Interstitial keratitis
Deep palmar branch of ulnar nerve	Structure of deep branch of ulnar nerve
Deep retinal hemorrhage	Deep retinal hemorrhage
Deep third degree burn of multiple sites of trunk	Full thickness burn of multiple sites of trunk
Deep transverse arrest	Deep transverse arrest
Deep transverse fibers of pons	Deep transverse fibers of pons
Deep vein thrombosis of leg related to air travel	Deep vein thrombosis of leg related to air travel
Deep vein thrombosis of leg related to air travel	Deep vein thrombosis of leg related to air travel
Deer fly	Genus Chrysops (organism)
Defaecating proctogram	Defaecating proctogram
déficiences de l'immunité humorale	Humoral immune defect
déficit en A-ase	Deficiency of asparaginase (disorder)
déficit en L-prolylglycine dipeptidase	Deficiency of cytosol non-specific dipeptidase
Deficiency of N-acetylgalactosamine-6-sulfatase	Deficiency of N-acetylgalactosamine-6-sulfatase
Deficiency of UDPglucose 4-epimerase	Galactose epimerase deficiency
Deficiency of acetyl-CoA carboxylase	Deficiency of acetyl-coenzyme A carboxylase (disorder)
Deficiency of acetylcholinesterase	Deficiency of acetylcholinesterase
Deficiency of acyl-CoA dehydrogenase	Acyl-CoA dehydrogenase deficiency
Deficiency of adenosine deaminase	Adenosine deaminase deficiency
Deficiency of adenylosuccinate lyase	Adenylosuccinate lyase deficiency
Deficiency of alkylhalidase	Deficiency of alkylhalidase (disorder)
Deficiency of alpha, alpha-trehalase	Trehalase deficiency
Deficiency of arginase	Arginase deficiency
Deficiency of argininosuccinate lyase	Argininosuccinate lyase deficiency
Deficiency of asparaginase	Deficiency of asparaginase (disorder)
déficit en benzoylcholinesterase	Deficiency of butyrylcholinesterase (disorder)
Deficiency of biotin	Biotin deficiency (disorder)
Deficiency of biotinidase	Biotinidase deficiency
Deficiency of butyrylcholine esterase	Deficiency of butyrylcholinesterase (disorder)
déficit en choline esterase I	Deficiency of acetylcholinesterase
Deficiency of cystathionine beta-synthase	Cystathionine beta-synthase deficiency
Deficiency of cystathionine gamma-lyase	Cystathionine gamma-lyase deficiency
Deficiency of cytochrome-c oxidase	Cytochrome-c oxidase deficiency
déficit en cytosol aminopeptidase	Deficiency of leucine aminopeptidase
Deficiency of cytosol aminopeptidase	Deficiency of leucine aminopeptidase
Deficiency of dihydropyrimidinase	Dihydropyrimidinase deficiency
Deficiency of dipeptidyl peptidase I	Deficiency of cathepsin C
Deficiency of dipeptidyl peptidase I	Deficiency of cathepsin C
Deficiency of dipeptidyl-amino-peptidase I	Deficiency of cathepsin C
Deficiency of folic acid (disorder)	Folic acid deficiency (disorder)
déficit en fumarate hydratase	Fumarate hydratase deficiency
Deficiency of glutamate-cysteine ligase	Glutamate-cysteine ligase deficiency
déficit en halogenase	Deficiency of alkylhalidase (disorder)
Deficiency of homogentisate 1,2-dioxygenase	Homogentisate 1,2-dioxygenase deficiency
déficit en hydroxymethylglutaryl-CoA lyase	Hydroxymethylglutaric aciduria (disorder)
déficit en imidodipeptidase	Deficiency of Xaa-Pro dipeptidase
déficit en iminodipeptidase	Deficiency of cytosol non-specific dipeptidase
déficit en inosinase	Deficiency of inosine nucleosidase
Deficiency of inosine nucleosidase	Deficiency of inosine nucleosidase
déficit en lecithinase D	Deficiency of phospholipase D
déficit en lipophosphodiesterase II	Deficiency of phospholipase D
déficit en long-chain fatty-acyl-CoA hydrolase	Deficiency of palmitoyl-coenzyme A hydrolase (disorder)
Deficiency of methylcrotonoyl-coenzyme A carboxylase	A rare inherited disorder of leucine metabolism characterised by a highly variable clinical picture ranging from metabolic crisis in infancy to asymptomatic adults.
Deficiency of ornithine-oxo-acid aminotransferase	Ornithine aminotransferase deficiency
Deficiency of palmitoyl-CoA hydrolase	Deficiency of palmitoyl-coenzyme A hydrolase (disorder)
Deficiency of pantothenic acid (disorder)	Pantothenic acid deficiency
déficit en pectin methoxylase	Deficiency of pectinesterase
déficit en pectin methylesterase	Deficiency of pectinesterase
Deficiency of pectinesterase	Deficiency of pectinesterase
Deficiency of phosphoenolpyruvate carboxykinase (GTP)	Phosphoenolpyruvate carboxykinase (GTP) deficiency
Deficiency of phospholipase D	Deficiency of phospholipase D
Deficiency of porphobilinogen synthase	Porphobilinogen synthase deficiency
Deficiency of proline dipeptidase	Deficiency of Xaa-Pro dipeptidase
déficit en proline dipeptidase	Deficiency of Xaa-Pro dipeptidase
Deficiency of prolyl dipeptidase	Deficiency of cytosol non-specific dipeptidase
déficit en prolyl dipeptidase	Deficiency of cytosol non-specific dipeptidase
Deficiency of pyruvate carboxylase	Pyruvate carboxylase deficiency
Deficiency of sucrase-isomaltase	Sucrase-isomaltase deficiency
Deficiency of sulfite oxidase	Sulfite oxidase deficiency
Deficiency of transhydroxymethylase	Deficiency of glycine hydroxymethyltransferase
Deficiency of triose-phosphate isomerase	Triose phosphate isomerase deficiency
Deficiency of true cholinesterase	Deficiency of acetylcholinesterase
Deficiency of vitamin B (disorder)	Vitamin B deficiency
Deficient perineum	Decreased anogenital distance
Deficient perineum	Decreased anogenital distance
Deficits in attention motor control and perception	Deficits in attention motor control and perception
Deflazacort	Product containing deflazacort (medicinal product)
Defloration	Non-virginal state
Deformation of breast	Deformation of breast
Deformation of breast	Deformation of breast
Deformed duodenal cap	Deformed duodenal cap (disorder)
Deformity after injury	Deformity after injury
déformation causée par une bride amniotique	Constriction rings syndrome is a congenital limb malformation disorder with an extremely variable clinical presentation characterized by the presence of partial to complete, congenital, fibrous, circumferential, constriction bands/rings on any part of the body, although a particular predilection for the upper or lower extremities is seen. Phenotypes range from only a mild skin indentation to complete amputation of parts of the fetus (e.g. digits, distal limb). Compression from the rings may lead to edema, skeletal anomalies (e.g. fractures, foot deformities) and, infrequently, neural compromise.
Deformity of bone (& acquired)	Deformation of bone
déformation d'un os	Deformation of bone
Deformity of bone of neck	Deformity of cervical vertebra
Deformity of bone of thoracic spine	Deformity of thoracic vertebra
Deformity of other tarsal bone (& acquired)	Deformation of bone
Deformity of other tarsal bone	Deformation of bone
Degenerated eye	Degenerative disorder of eye
Degenerated globe	Degenerative disorder of eye
dégénérescence	Degenerative abnormality
Degeneration of papillary muscle	Papillary muscle degeneration

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Reference Sets

Reference set descriptor

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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)