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
kongenital minskad cellularitet	Hypoplasia
Congenital deformity of sacroiliac joint	Congenital deformity of sacroiliac joint
kongenital degeneration	Degenerative abnormality (morphologic abnormality)
kongenital utvecklingsanomali	Morphologically abnormal structure (morphologic abnormality)
kongenital deviation	Displacement
kongenital dilatation	Dilatation
Congenital dilatation of aorta	Congenital dilatation of aorta
Congenital dilatation of ureter	Congenital dilatation of ureter (disorder)
Congenital dilatation of ureter (disorder)	Disorder of coccyx
medfödd gallgångsdilatation	Congenital dilatation of common bile duct (disorder)
medfödd diplegi	Diplegic cerebral palsy
Congenital discoid meniscus	Congenital discoid meniscus
Congenital discoid meniscus	Congenital discoid meniscus
medfödd luxation	Dislocation
Congenital dislocation of elbow	Congenital dislocation of elbow (disorder)
Congenital dislocation of hip NOS	Congenital dislocation of hip NOS
Congenital dislocation of hip NOS	Congenital dislocation of hip NOS
Congenital dislocation of patella	Congenital dislocation of patella
Congenital dislocation of the hip screening	Congenital dislocation of the hip screening
Congenital disorder	Congenital disease (disorder)
medfödd förskjutning av njure	Congenital malposition of kidney
Congenital displacement of esophagus	Congenital displacement of esophagus
kongenital dislokation av magsäcksslemhinna	Ectopic gastric mucosa
Congenital diverticulum of colon	Congenital diverticulum of colon
Congenital diverticulum of oesophagus	Congenital diverticulum of esophagus
Congenital dyserythropoietic anaemia type II	Congenital dyserythropoietic anemia, type II
kongenital dysfagocytos	Chronic granulomatous disease (disorder)
kongenital dysplasi	Dysplasia
Congenital dysplasia of the hip	Congenital hip dysplasia
kongenital dystrofi	Dystrophic atrophy
Congenital elevation of scapula	Congenital elevation of scapula
kongenital elliptocytos	Hereditary elliptocytosis
Congenital enlarged kidney	Large kidney
medfödd förstoring	Enlargement (morphologic abnormality)
Congenital epiblepharon-inferior oblique syndrome	Congenital epiblepharon-inferior oblique syndrome
medfött navelbråck	Congenital omphalocele
medfödd extensionsdeformitet	Extension deformity
Congenital eye disorder screening	Congenital eye disorder screening
Congenital factor IX deficiency	Hereditary factor IX deficiency disease
medfödd utebliven fusion	Developmental failure of fusion (morphologic abnormality)
Congenital falciparum malaria	Congenital falciparum malaria
Congenital fiber type disproportion myopathy	Congenital myopathy with fibre type disproportion
Congenital fissure of epiglottis	Congenital fissure of epiglottis
medfödd fissur i larynx	Congenital cleft larynx
medfödd fissur i tungan	Plicated tongue
medfödd fistel	Fistula
Congenital fistula of auricle	Preauricular fistula
Congenital fistula of salivary gland	Congenital salivary gland fistula
medfödd flexionsdeformitet	Flexion deformity
kongenital fokal hypertrofi	Focal hypertrophy
medfödda veck i bakre ögonkammare	Congenital fold of posterior segment of eye
Congenital forehead deformity	Congenital deformity of forehead
kongenital framåtriktad deviation	Anterior displacement
medfödd fraktur	Fracture
Congenital fusion of ear ossicles	Congenital fusion of ossicles of ear
Congenital fusion of kidneys	Fusion of kidneys (disorder)
Congenital fusion of labia	Congenital fusion of labia
Congenital glaucoma	Congenital glaucoma
medfödd tillväxtförändring	Growth alteration
hamartos	Congenital hamartoma (disorder)
Congenital heart block	Congenital heart block
Congenital heart block	Congenital heart block
kongenital hemangioblastomatos	Hemangioblastomatosis
medfött hemangiom	Benign hemangioma
kongenital hemangiomatos	Hemangiomatosis
kongenital hemihypertrofi	Hypertrophy
Congenital hepatitis B infection	Congenital viral hepatitis B infection
Congenital hepatomegaly	Congenital hepatomegaly
Congenital hereditary muscular dystrophy	Congenital hereditary muscular dystrophy
Congenital hernia of bladder	Congenital bladder hernia (disorder)
medfött bråck i foramen Bochdalek	Congenital posterolateral diaphragmatic hernia (disorder)
Congenital hydrocephalus	Congenital hydrocephalus
Congenital hydronephrosis	Congenital hydronephrosis
kongenital hyperpigmentering	Hyperpigmentation
kongenital hyperplasi	Hyperplasia
kongenital hypertrofi	Hypertrophy
kongenital hypopigmentering	Hypopigmentation
kongenital hypoplasi	Hypoplasia
Congenital hypoplasia of bile duct	Congenital hypoplasia of bile duct
Congenital hypothyroidism	Endemic cretinism
Congenital hypothyroidism with diffuse goitre	Congenital hypothyroidism with diffuse goitre
Congenital hypothyroidism with diffuse goitre	Congenital hypothyroidism with diffuse goitre
Congenital hypothyroidism without goitre	Congenital hypothyroidism without goitre
höggradig kongenital imperforation	Congenital atresia
låggradig kongenital imperforation	Congenital atresia
medfött inkomplett atrioventrikulärt block	Congenital incomplete atrioventricular heart block
Congenital incomplete closure	Developmental failure of fusion (morphologic abnormality)
Congenital insufficiency of the pulmonary valve	Congenital insufficiency of pulmonary valve
Congenital integument anomalies (& [birthmark NOS])	Congenital anomaly of integument
Congenital intestinal adhesions NOS	Adhesion
kongenital invagination	Invagination
Congenital iodine deficiency hypothyroidism	Endemic cretinism
Congenital iodine deficiency syndrome	Endemic cretinism
Congenital iodine deficiency syndrome - mixed type	Congenital iodine deficiency syndrome of mixed type (disorder)
Congenital iodine deficiency syndrome - myxoedematous type	Endemic cretinism
Congenital iodine deficiency syndrome - myxoedematous type	Endemic cretinism
Congenital iodine deficiency syndrome - neurological type	Congenital iodine deficiency syndrome of neurological type (disorder)
kongenital keratincysta	Keratinizing cyst (morphologic abnormality)
Congenital keratoconus	Congenital keratoconus
Congenital keratoderma	Congenital keratoderma
medfödda labiala adherenser	Congenital labial adhesion

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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)