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)	est un(e) (attribut)	Historical association reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	targetComponentId
(Congenital dislocation of hip) or (clicky hips) or (subluxation of hip - congenital)	luxation congénitale d'une hanche
(Congenital dislocation of hip) or (clicky hips) or (subluxation of hip - congenital)	Congenital subluxation of hip
(Congenital ectodermal defect) or (integument anomalies NOS) (disorder)	Congenital ectodermal defect
(Congenital generalised alopecia) or (atrichosis) (disorder)	Congenital generalised alopecia
(Congenital genital anomaly NOS) or (pseudohermaphroditism) (disorder)	Pseudohermaphroditism
(Congenital genital anomaly NOS) or (pseudohermaphroditism)	Congenital malformation of genital organs
(Congenital genital anomaly NOS) or (pseudohermaphroditism)	Pseudohermaphroditism
(Congenital heart anomaly NOS) or (Chiari's malformation) (disorder)	Chiari's network
(Congenital heart anomaly NOS) or (valve - congenital heart) or (valvular heart disease, congenital)	maladie cardiaque congénitale
(Congenital heart anomaly NOS) or (valve - congenital heart) or (valvular heart disease, congenital) (disorder)	maladie cardiaque congénitale
(Congenital heart anomaly NOS) or (valve - congenital heart) or (valvular heart disease, congenital)	Congenital anomaly of heart valve
(Congenital heart disease, septal and bulbar anomalies) or (bulbus cordis and cardiac septal closure anomalies) or (septal defects: [heart] or [cardiac]) (disorder)	Bulbus cordis and cardiac septal closure anomalies
(Congenital heart disease, septal and bulbar anomalies) or (bulbus cordis and cardiac septal closure anomalies) or (septal defects: [heart] or [cardiac]) (disorder)	Cardiac septal defects
(Congenital heart disease, septal and bulbar anomalies) or (bulbus cordis and cardiac septal closure anomalies) or (septal defects: [heart] or [cardiac]) (disorder)	Congenital heart disease, septal and bulbar anomalies
(Congenital hydrocele) or (patent processus vaginalis) (disorder)	Patent processus vaginalis
(Congenital hydrocele) or (patent processus vaginalis) (disorder)	Congenital hydrocele
(Congenital ichthyosiform erythroderma) or (alligator skin) or (ichthyosis congenita NOS)	Congenital ichthyosiform erythroderma
(Congenital kyphosis) or (Patau's syndrome NOS) (disorder)	Complete trisomy 13 syndrome
(Congenital kyphosis) or (Patau's syndrome NOS) (disorder)	cyphose acquise
(Congenital kyphosis) or (Patau's syndrome NOS)	déformation cyphotique de la colonne vertébrale
(Congenital kyphosis) or (Patau's syndrome NOS) (disorder)	Congenital kyphosis
(Congenital kyphosis) or (Patau's syndrome NOS)	Congenital kyphosis
(Congenital kyphosis) or (Patau's syndrome NOS) (disorder)	déformation cyphotique de la colonne vertébrale
(Congenital kyphosis) or (Patau's syndrome NOS)	cyphose acquise
(Congenital kyphosis) or (Piere-Robin syndrome)	cyphose acquise
(Congenital kyphosis) or (Piere-Robin syndrome)	Robin sequence (disorder)
(Congenital kyphosis) or (Piere-Robin syndrome) (disorder)	cyphose acquise
(Congenital kyphosis) or (Piere-Robin syndrome) (disorder)	Robin sequence (disorder)
(Congenital kyphosis) or (Piere-Robin syndrome)	déformation cyphotique de la colonne vertébrale
(Congenital kyphosis) or (Piere-Robin syndrome) (disorder)	Congenital kyphosis
(Congenital kyphosis) or (Piere-Robin syndrome) (disorder)	déformation cyphotique de la colonne vertébrale
(Congenital kyphosis) or (Piere-Robin syndrome)	Congenital kyphosis
(Congenital limb deformity NOS) or (pes cavus) or (claw toe) or (dysmorphic toes) or (Larsen's syndrome) (disorder)	Talipes cavus (disorder)
(Congenital limb deformity NOS) or (pes cavus) or (claw toe) or (dysmorphic toes) or (Larsen's syndrome)	Acquired claw toes
(Congenital limb deformity NOS) or (pes cavus) or (claw toe) or (dysmorphic toes) or (Larsen's syndrome)	Larsen syndrome
(Congenital limb deformity NOS) or (pes cavus) or (claw toe) or (dysmorphic toes) or (Larsen's syndrome) (disorder)	Larsen syndrome
(Congenital limb deformity NOS) or (pes cavus) or (claw toe) or (dysmorphic toes) or (Larsen's syndrome)	Talipes cavus (disorder)
(Congenital limb deformity NOS) or (pes cavus) or (claw toe) or (dysmorphic toes) or (Larsen's syndrome) (disorder)	Acquired claw toes
(Congenital malposition of digestive system NOS) or (ectopic digestive organs NOS) (disorder)	Congenital anomaly of digestive system
(Congenital megalocornea) or (enlarged cornea) or (congenital macrocornea) (disorder)	Megalocornea
(Congenital monilethrix) or (beaded hair) (disorder)	Beaded hair
(Congenital monoplegia) or (congenital spastic foot) (disorder)	paralysie cérébrale monoplégique
(Congenital monoplegia) or (congenital spastic foot) (disorder)	Congenital spastic foot
(Congenital musculoskeletal anomalies NOS) or (congenital deformity of musculoskeletal system NEC) (disorder)	Congenital anomaly of musculoskeletal system
(Congenital pachyonychia) or (hypertrophic nails) (disorder)	Pachyonychia congenita syndrome
(Congenital pes planus) or (flat foot: [congenital] or [rigid] or [spastic]) (disorder)	pied plat congénital
(Congenital pes planus) or (flat foot: [congenital] or [rigid] or [spastic]) (disorder)	Rigid flat foot
(Congenital ptosis) or (blepharoptosis) (disorder)	Congenital ptosis of upper eyelid
(Congenital renal failure) or (congenital uraemia) (disorder)	Congenital uraemia
(Congenital renal failure) or (congenital uraemia) (disorder)	Congenital renal failure
(Congenital respiratory anomalies NOS) or (bronchiectasis - congenital) (disorder)	Congenital malformation of the respiratory system
(Congenital respiratory anomalies NOS) or (bronchiectasis - congenital) (disorder)	Congenital bronchiectasis
(Congenital shortening of arm, unspecified) or (brachymelia of arm) (disorder)	déformation associée à une réduction d'un membre supérieur
(Congenital spine deformity NOS) or (congenital postural curvature of spine NOS) (disorder)	Congenital deformity of spine
(Congenital spine deformity NOS) or (congenital postural curvature of spine NOS) (disorder)	scoliose posturale congénitale
(Congenital spine deformity NOS) or (congenital postural curvature of spine NOS) (disorder)	Congenital kyphosis
(Congenital spine deformity NOS) or (congenital postural curvature of spine NOS) (disorder)	Congenital lordosis deformity of spine (disorder)
(Congenital sternomastoid torticollis) or (congenital wry neck) or (sternomastoid tumour) (disorder)	torticolis congénital
(Congenital talipes varus) or (pes varus) or (congenital clubfoot - varus) (disorder)	Congenital varus deformity of foot
(Congenital talipes varus) or (pes varus) or (congenital clubfoot - varus) (disorder)	Adductus deformity of foot
(Congenital toxoplasmosis (& [lymphadenopathy due to]) or (congenital hydrocephalus due to toxoplasmosis) (disorder)	Congenital toxoplasmosis
(Congenital toxoplasmosis (& [lymphadenopathy due to]) or (congenital hydrocephalus due to toxoplasmosis) (disorder)	hydrocéphalie causée par une toxoplasmose congénitale
(Congenital toxoplasmosis (& [lymphadenopathy due to]) or (congenital hydrocephalus due to toxoplasmosis) (disorder)	lymphoadénopathie causée par une toxoplasmose congénitale
(Congenital ureter anomaly NOS) or (ureter anomaly - congenital) (disorder)	Congenital anomaly of ureter (disorder)
(Congenital ureter anomaly NOS) or (ureter anomaly - congenital)	Congenital anomaly of ureter (disorder)
(Congenital ureteric valves) or (occlusion of ureter) (disorder)	Congenital ureteric valves
(Congenital ureteric valves) or (occlusion of ureter) (disorder)	Occlusion of ureter
(Congenital) circulation: [fetal] or [system anomaly NOS (& acquired)] (disorder)	Congenital anomaly of cardiovascular system
(Congenital) nipple: [small (& acquired)] or [hypoplasia]	Hypoplasia of nipple
(Congenital) nipple: [small (& acquired)] or [hypoplasia]	Small nipple
(Congenital) occlusion of anus or (congenital/acquired) anal septum (disorder)	Congenital occlusion of anus
(Congenital) or (acquired) aberrant thyroid gland (& [retrosternal])	Aberrant thyroid gland
(Congenital) or (acquired) aberrant thyroid gland (& [retrosternal])	Retrosternal thyroid gland
(Congenital) or (acquired) absent nose (disorder)	Congenital absence of nose
(Congenital) or (acquired) absent thumb (disorder)	Thumb absent
(Congenital) or (acquired) anomaly: [msk] or [skeletal] (disorder)	Congenital anomaly of musculoskeletal system
(Congenital) or (acquired) cystic kidney disease (& [cyst] or [polycystic] or [fibrocystic] kidney) (disorder)	Multiple congenital cysts of kidney
(Congenital) or (acquired) cystic kidney disease (& [cyst] or [polycystic] or [fibrocystic] kidney)	Multiple congenital cysts of kidney
(Congenital) or (acquired) diaphragm anomaly (& eventration)	Congenital eventration of diaphragm
(Congenital) or (acquired) diaphragm anomaly (& eventration) (disorder)	Congenital eventration of diaphragm
(Congenital) or (acquired) diaphragm anomaly (& eventration)	Congenital anomaly of diaphragm
(Congenital) or (acquired) diaphragm anomaly (& eventration) (disorder)	Congenital anomaly of diaphragm
(Congenital) or (acquired) fusion: [vulva] or [labia] (disorder)	Fusion of vulva
(Congenital) or (acquired) lung cyst (& [bronchogenic]) (disorder)	Congenital bronchogenic cyst
(Congenital) or (acquired) palmaris et plantaris: [keratosis] or [tylosis] (disorder)	kératose
(Congenital) or (acquired) palmaris et plantaris: [keratosis] or [tylosis] (disorder)	kératodermie palmaire et plantaire acquise (trouble)
(Congenital) or (acquired) palmaris et plantaris: [keratosis] or [tylosis] (disorder)	Hereditary diffuse palmoplantar keratoderma (disorder)
(Congenital) or (acquired) palmaris et plantaris: [keratosis] or [tylosis] (disorder)	Diffuse palmoplantar keratoderma of Thost-Unna (disorder)
(Congenital) or (acquired) palmaris et plantaris: [keratosis] or [tylosis] (disorder)	Keratoderma climactericum (disorder)
(Congenital) or (acquired) pharyngeal pouch (disorder)	Congenital diverticulum of pharynx
(Congenital) or (acquired) splenomegaly (disorder)	splénomégalie congénitale
(Congenital) or (acquired) tongue: [bifid] or [fissure] (disorder)	Bifid tongue
(Congenital) or (acquired) tongue: [bifid] or [fissure] (disorder)	Plicated tongue (disorder)
(Congenital): [macroglossia (& acquired)] or [tongue hypertrophy] (disorder)	Enlargement of tongue
(Congenital): [macroglossia (& acquired)] or [tongue hypertrophy] (disorder)	macroglossie congénitale
(Congenital): [macroglossia (& acquired)] or [tongue hypertrophy] (disorder)	Acquired macroglossia (disorder)
(Congenital: [polycystic lung] or [multiple bronchogenic cysts]) or (multiple lung cysts) (disorder)	Multiple cysts of lung (disorder)
(Congenital: [polycystic lung] or [multiple bronchogenic cysts]) or (multiple lung cysts) (disorder)	Congenital cystic lung
(Congestive cardiac failure) or (dropsy) or (cardiac insufficiency) or (right heart failure) or (right ventricular failure)	Heart failure
(Congestive cardiac failure) or (dropsy) or (cardiac insufficiency) or (right heart failure) or (right ventricular failure) (disorder)	Right ventricular failure
(Congestive cardiac failure) or (dropsy) or (cardiac insufficiency) or (right heart failure) or (right ventricular failure)	Biventricular congestive heart failure

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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)