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
Congenital bronchomalacia	Congenital bronchomalacia
Congenital calculus of kidney	Congenital calculus of kidney
Congenital camptodactyly	Camptodactyly
Congenital cardiomegaly	Congenital cardiomegaly
Congenital cataract	Congenital cataract
Congenital cavitation	Cystic dilatation
Congenital chorioretinal degeneration	Congenital chorioretinal degeneration
Congenital claw toe	Congenital claw toe
Congenital cleft larynx and Opitz-Frias syndrome	Opitz-Frias syndrome
Congenital clubbing	Congenital clubnail
Congenital colloid cyst	Colloid cyst
Congenital complete atrioventricular block	Congenital complete atrioventricular heart block
Congenital complete heart block	Congenital complete atrioventricular heart block
Congenital contracture	Contracture
Congenital convex pes valgus	Congenital vertical talus (disorder)
Congenital cyst of canal of Nuck	Congenital cyst of canal of Nuck
kyste congénital d'une trompe utérine	Embryonic cyst of fallopian tube
Congenital cyst of kidney	Congenital renal cyst (disorder)
Congenital cyst of ovary	Embryonic cyst of ovary
Congenital cyst of spleen	Congenital cyst of spleen
Congenital cyst of urachus	Allantoic cyst
Congenital cyst of vulva	Congenital cyst of vulva
Congenital cystic disease of kidney	Congenital cystic kidney disease
Congenital cystic liver disease	Congenital cystic disease of liver
Congenital cystic lung	Congenital cystic lung
Congenital decrease in cellularity	Hypoplasia
Congenital deficiency of pancreatic lipase	Pancreatic triacylglycerol lipase deficiency
Congenital deformity of sacroiliac joint	Congenital deformity of sacroiliac joint (disorder)
Congenital degeneration	Degenerative abnormality
anomalie congénitale du développement	Morphologically abnormal structure
Congenital deviation	Displacement
Congenital dilatation	Dilatation
Congenital dilatation of aorta	Congenital dilatation of aorta
Congenital dilatation of ureter (disorder)	Disorder of coccyx
Congenital dilatation of ureter	Congenital dilatation of ureter (disorder)
Congenital dilation of bile duct	Congenital dilatation of common bile duct (disorder)
diplégie congénitale	A form of spastic cerebral palsy affecting two limbs; usually the legs are affected more than the arms.
ménisque discoïde congénital	Congenital discoid meniscus of knee (disorder)
Congenital discoid meniscus	Congenital discoid meniscus of knee (disorder)
Congenital discoid meniscus	Congenital discoid meniscus of knee (disorder)
Congenital dislocation	Dislocation
Congenital dislocation of elbow	Congenital dislocation of elbow (disorder)
Congenital dislocation of patella	Congenital dislocation of patella
Congenital dislocation of the hip screening	Congenital dislocation of the hip screening
Congenital disorder	Congenital disease
Congenital displaced kidney	Congenital malposition of kidney
Congenital displacement of esophagus	Congenital displacement of esophagus
Congenital displacement of gastric mucosa	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
Congenital dysphagocytosis	Chronic granulomatous disease (disorder)
Congenital dysplasia	Dysplasia
Congenital dysplasia of the hip	Congenital hip dysplasia
Congenital dystrophy	Dystrophic atrophy
Congenital elevation of scapula	Congenital elevation of scapula
elliptocytose congénitale	Hereditary elliptocytosis
Congenital enlarged kidney	Large kidney
Congenital enlargement	Enlargement (morphologic abnormality)
Congenital epiblepharon-inferior oblique syndrome	Congenital epiblepharon-inferior oblique syndrome
exomphale congénitale	Congenital omphalocele
Congenital extension deformity	Extension deformity
Congenital eye disorder screening	Congenital eye disorder screening
Congenital factor IX deficiency	Hereditary factor IX deficiency disease
Congenital failure of fusion	Developmental failure of fusion (morphologic abnormality)
Congenital falciparum malaria	Congenital falciparum malaria
Congenital fiber type disproportion myopathy	A rare genetic, congenital, non-dystrophic myopathy characterized by neonatal or infantile-onset hypotonia and mild to severe generalized muscle weakness.
Congenital fissure of epiglottis	Congenital fissure of epiglottis
Congenital fissure of larynx	Congenital cleft larynx
Congenital fissure of tongue	Plicated tongue
Congenital fistula	Fistula
Congenital fistula of auricle	Preauricular fistula
Congenital fistula of salivary gland	Congenital salivary gland fistula
Congenital fistula of urachus (disorder)	Congenital fistula of urachus
Congenital fistula of urachus	Congenital fistula of urachus
Congenital flexion deformity	Flexion deformity
Congenital focal hypertrophy	Focal hypertrophy (morphologic abnormality)
Congenital folds of the posterior segment	Congenital fold of posterior segment of eye
Congenital forehead deformity	Congenital deformity of forehead
Congenital forward deviation	Anterior displacement
Congenital fracture	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
malabsorption congénitale du glucose-galactose	Glucose-galactose malabsorption (disorder)
Congenital growth alteration	Growth alteration
Congenital hamartosis	Congenital hamartoma (disorder)
Congenital heart block	Congenital heart block
Congenital heart block	Congenital heart block
Congenital hemangioblastomatosis	Hemangioblastomatosis
Congenital hemangioma	Benign hemangioma
Congenital hemangiomatosis	Hemangiomatosis
Congenital hemihypertrophy	Hypertrophy
Congenital hepatitis B infection	Congenital viral hepatitis B infection
Congenital hepatomegaly	Congenital hepatomegaly
Congenital hereditary muscular dystrophy	Congenital hereditary muscular dystrophy (disorder)
Congenital hernia of bladder	Congenital hernia of urinary bladder (disorder)
Congenital hernia of foramen of Bochdalek	Congenital posterolateral diaphragmatic hernia (disorder)
Congenital hydrocephalus	Congenital hydrocephalus
Congenital hydronephrosis	Congenital hydronephrosis

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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)