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 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 left hip	Developmental dysplasia of left hip
Congenital dysplasia of right hip	Developmental dysplasia of right hip
Congenital dysplasia of the hip	Congenital hip dysplasia
Congenital dystrophy	Dystrophic atrophy
Congenital elevation of scapula	Congenital elevation of scapula
Congenital elliptocytosis	Hereditary elliptocytosis
Congenital enlarged kidney	Large kidney
Congenital enlargement	Enlargement (morphologic abnormality)
Congenital epiblepharon-inferior oblique syndrome	Congenital epiblepharon-inferior oblique syndrome
Congenital exomphalos	Congenital omphalocele
Congenital extension deformity	Extension deformity (morphologic abnormality)
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	Congenital myopathy with fibre type disproportion
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
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
Congenital glaucoma of left eye	Congenital glaucoma of left eye
Congenital glucose-galactose malabsorption	Glucose-galactose malabsorption
Congenital growth alteration	Growth alteration
Congenital hallux valgus of bilateral great toes	Bilateral congenital hallux valgus
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
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
Congenital hyperpigmentation	Hyperpigmentation
Congenital hyperplasia	Hyperplasia
Congenital hypertrophy	Hypertrophy
Congenital hypopigmentation	Hypopigmentation
Congenital hypoplasia	Hypoplasia
Congenital hypoplasia of bile duct	Congenital hypoplasia of bile duct
Congenital hypoplasia of umbilical artery	Congenital hypoplasia of umbilical artery
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
Congenital incomplete atrioventricular 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
Congenital 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)
Congenital keratin cyst	Keratinizing cyst (morphologic abnormality)
Congenital keratoconus	Congenital keratoconus
Congenital keratoderma	Congenital keratoderma
Congenital labial adhesions	Congenital labial adhesion
Congenital lacrimal gland anomalies	Congenital anomaly of lacrimal gland
Congenital laryngeal abductor palsy	Congenital laryngeal abductor palsy
Congenital laryngeal adductor palsy	Congenital laryngeal adductor palsy
Congenital laryngeal atresia	Congenital atresia of larynx
Congenital lateral deviation	Lateral displacement
Congenital lens anomaly	Congenital anomaly of lens
Congenital lipoatrophic diabetes	Congenital total lipodystrophy (disorder)
Congenital lipoatrophic diabetes	Congenital total lipodystrophy (disorder)
Congenital livedo reticularis	Congenital livedo reticularis
Congenital lobar emphysema	Congenital emphysema
Congenital luminal atresia of aortic arch	Congenital atresia of aortic arch (disorder)
Congenital lymphangiectasis	Lymphangiectasis
Congenital lymphangioma	Congenital lymphangioma
Congenital lymphangiomatosis	Lymphangiomatosis
Congenital malformation of genital organs	Congenital malformation of genital organs (disorder)
Congenital malformation of genital organs	Congenital malformation of genital organs (disorder)
Congenital malformation of knee	Congenital deformity of knee joint
Congenital malformation of lacrimal gland	Congenital anomaly of lacrimal system

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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)