900000000000523009: POSSIBLY EQUIVALENT TO 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)\POSSIBLY EQUIVALENT TO 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

900000000001150016 POSSIBLY EQUIVALENT TO 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)
900000000001151017 POSSIBLY EQUIVALENT TO 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
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)	Is a	Historical association reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	targetComponentId
Congenital diaphragmatic: [hernia] or [defect NEC]	Congenital diaphragmatic hernia
Congenital diplegia	Diplegic cerebral palsy
Congenital diplegia	Paraplegic cerebral palsy (disorder)
medfödd sjukdom och abnormitet i hjärta, bröstaorta och perikardium	Multiple system malformation syndrome
medfödd luxation och subluxation i höft	Congenital dislocation of hip
Congenital dislocation of elbow	Dislocation of joint of upper limb
Congenital dislocation of elbow	Congenital dislocation of elbow (disorder)
medfödda störningar av öga och ögonlocksrörelser	Movement of eyelid - finding
medfödda störningar av öga och ögonlocksrörelser	Congenital anomaly of eyelid
medfödda störningar av öga och ögonlocksrörelser	Congenital anomaly of eye
Congenital displaced uterus (& [prolapse])	Congenital prolapsed uterus
Congenital displaced uterus (& [prolapse])	Malposition of uterus
Congenital diverticulum of esophagus	Congenital diverticulum of esophagus
Congenital dystrophia brevicollis	Congenital dystrophia brevicollis (disorder)
Congenital dystrophia brevicollis	Turner syndrome
kongenital ektodermal dysplasi av ansikte	Focal facial dermal dysplasia (disorder)
Congenital ectopia (morphologic abnormality)	Congenital ectopia (morphologic abnormality)
Congenital ectopia (morphologic abnormality)	Choristoma (morphologic abnormality)
Congenital epiblepharon-inferior oblique syndrome	Congenital epiblepharon-inferior oblique syndrome
Congenital epiblepharon-inferior oblique syndrome	Swan's syndrome II
Congenital epulis of newborn	Congenital gingival granular cell tumor
Congenital epulis of newborn	Congenital epulis of newborn
Congenital exostosis (& [multiple])	Multiple congenital exostosis
Congenital exostosis (& [multiple])	Congenital exostosis
Congenital face or neck anomaly NOS	Congenital anomaly of face (disorder)
Congenital face or neck anomaly NOS	Congenital anomaly of neck
medfödd utebliven fusion med bråck	Developmental failure of fusion (morphologic abnormality)
medfödd dystrofi i ansikte	Stiff skin syndrome
Congenital fusion of spine (& [lumbosacral])	Congenital fusion of spine
Congenital fusion of spine (& [lumbosacral])	Congenital lumbosacral fusion
medfött pigmenterat jättenevus i hud	Congenital benign giant pigmented nevus of skin (disorder)
medfött pigmenterat jättenevus i hud	Giant pigmented naevus of skin
Congenital glaucoma	Buphthalmos (finding)
Congenital glaucoma	Buphthalmos (finding)
Congenital glaucoma	Primary congenital glaucoma (disorder)
Congenital glaucoma	Primary congenital glaucoma (disorder)
Congenital hallux valgus	Congenital hallux valgus
Congenital hallux valgus	Hallux valgus
Congenital heart and cardiac apex malposition (& [ectopic heart])	Ectopia cordis
Congenital heart and cardiac apex malposition (& [ectopic heart])	Congenital malposition of heart
Congenital heart anomaly NOS	Congenital heart disease
Congenital heart anomaly NOS	Congenital heart disease
medfödd hyperammonemi typ 1	Carbamoyl-phosphate synthetase 1 deficiency (disorder)
medfödd hyperrotation	Congenital malrotation (morphologic abnormality)
kongenital hypodonti av flera tänder i samband med systemsjukdom	Partial congenital absence of teeth
kongenital hypodonti av flera tänder i samband med systemsjukdom	Anodontia
kongenital hypodonti av flera tänder utan samband med systemsjukdom	Partial congenital absence of teeth
kongenital hypodonti av flera tänder utan samband med systemsjukdom	Anodontia
Congenital hypoplasia of renal papilla	Congenital hypoplasia of renal papilla
Congenital hypoplasia of renal papilla	Congenital small renal papilla
Congenital hypothyroidism: [cretinism] or [NOS]	Congenital hypothyroidism
Congenital hypotonia	Neonatal hypotonia
Congenital hypotonia	Floppy infant syndrome
Congenital infection: [NOS] or [cytomegalovirus] or [herpes simplex] or [toxoplasmosis]	Congenital cytomegalovirus infection
Congenital infection: [NOS] or [cytomegalovirus] or [herpes simplex] or [toxoplasmosis]	Congenital cytomegalovirus infection
Congenital infection: [NOS] or [cytomegalovirus] or [herpes simplex] or [toxoplasmosis]	Congenital toxoplasmosis
Congenital infection: [NOS] or [cytomegalovirus] or [herpes simplex] or [toxoplasmosis]	Congenital toxoplasmosis
Congenital integument anomalies (& [birthmark NOS])	Congenital anomaly of integument
Congenital kyphoscoliosis	Congenital kyphoscoliosis (disorder)
Congenital kyphoscoliosis	Acquired kyphoscoliosis (disorder)
Congenital kyphoscoliosis	Kyphoscoliosis deformity of spine (disorder)
Congenital kyphosis	Congenital kyphosis
Congenital kyphosis	Acquired kyphosis (disorder)
Congenital kyphosis	Kyphosis deformity of spine (disorder)
Congenital lens: [ectopic] or [displaced] or [dislocation]	Congenital ectopic lens
Congenital limb deformities (& [Madelung's wrist])	Congenital anomaly of limb
Congenital limb deformities (& [Madelung's wrist])	Congenital anomaly of limb
Congenital limb deformities (& [Madelung's wrist])	Leri-Weill dyschondrosteosis
Congenital limb deformities (& [Madelung's wrist])	Madelung's deformity
Congenital lip: [fistula] or [pits]	Congenital lip pits
Congenital lip: [fistula] or [pits]	Congenital fistula of lip
Congenital lipoatrophic diabetes	Congenital total lipodystrophy (disorder)
Congenital lobar emphysema	Congenital lobar emphysema
Congenital lordosis &/or scoliosis	Congenital lordosis deformity of spine (disorder)
Congenital lordosis &/or scoliosis	Congenital postural scoliosis
Congenital lordosis &/or scoliosis	Congenital lordosis deformity of spine (disorder)
Congenital lordosis &/or scoliosis	Congenital postural scoliosis
Congenital lordosis &/or scoliosis	Congenital lordosis and scoliosis deformity of spine (disorder)
Congenital lordosis &/or scoliosis	Congenital lordosis and scoliosis deformity of spine (disorder)
Congenital lymphoedema	Hereditary lymphedema type I (disorder)
Congenital lymphoedema	Hereditary lymphedema
medfödda förändringar i makula	Congenital anomaly of macula
medfödd missbildning	Morphologically abnormal structure (morphologic abnormality)
Congenital malformation of the skin	Congenital anomaly of integument
Congenital malformation of the skin	Congenital anomaly of skin
Congenital malformation syndrome affecting facial appearance NOS	Multiple malformation syndrome with facial defects as major feature
Congenital malformation syndrome affecting facial appearance NOS	Congenital anomaly of face (disorder)
medfött missbildningssyndrom orsakat av känd exogen faktor	Congenital malformation syndrome (disorder)
Congenital malformation syndrome involving limbs NOS	Congenital anomaly of limb
Congenital malformation syndrome involving limbs NOS	Multiple malformation syndrome with limb defect as major feature
Congenital malformation syndrome with metabolic disturbance NOS	Metabolic disease
Congenital malformation syndrome with metabolic disturbance NOS	Congenital malformation syndrome (disorder)
Congenital malformation syndrome with metabolic disturbance NOS	Inborn error of metabolism
Congenital malformation syndromes due to known exogenous causes	Congenital malformation syndrome (disorder)
medfödda missbildningssyndrom med störd metabolism	Inborn error of metabolism
medfödda missbildningssyndrom med störd metabolism	Metabolic disease
medfödda missbildningssyndrom med störd metabolism	Congenital malformation syndrome (disorder)
Congenital melanocytic nevus	Congenital pigmented melanocytic nevus of skin (disorder)
Congenital melanocytic nevus	Congenital pigmented melanocytic nevus (disorder)
Congenital meningocele	Meningocele (disorder)
Congenital meningocele	Congenital meningocele

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
900000000001150016	POSSIBLY EQUIVALENT TO 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)
900000000001151017	POSSIBLY EQUIVALENT TO association reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)