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 kyphosis) or (Patau's syndrome NOS)	Acquired kyphosis (disorder)
(Congenital kyphosis) or (Patau's syndrome NOS)	Acquired kyphosis (disorder)
(Congenital kyphosis) or (Patau's syndrome NOS)	Kyphosis deformity of spine (disorder)
(Congenital kyphosis) or (Patau's syndrome NOS)	Congenital kyphosis
(Congenital kyphosis) or (Piere-Robin syndrome)	Acquired kyphosis (disorder)
(Congenital kyphosis) or (Piere-Robin syndrome)	Kyphosis deformity of spine (disorder)
(Congenital kyphosis) or (Piere-Robin syndrome)	Robin sequence
(Congenital kyphosis) or (Piere-Robin syndrome)	Robin sequence
(Congenital kyphosis) or (Piere-Robin syndrome)	Congenital kyphosis
(Congenital kyphosis) or (Piere-Robin syndrome)	Kyphosis deformity of spine (disorder)
(Congenital kyphosis) or (Piere-Robin syndrome)	Acquired kyphosis (disorder)
(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)	Larsen syndrome
(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)	Talipes cavus
(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)	Talipes cavus
(Congenital limb deformity NOS) or (pes cavus) or (claw toe) or (dysmorphic toes) or (Larsen's syndrome)	Larsen syndrome
(Congenital malposition of digestive system NOS) or (ectopic digestive organs NOS)	Congenital anomaly of digestive system
(Congenital megalocornea) or (enlarged cornea) or (congenital macrocornea)	Megalocornea
(Congenital monilethrix) or (beaded hair)	Beaded hair
(Congenital monoplegia) or (congenital spastic foot)	Congenital spastic foot
(Congenital monoplegia) or (congenital spastic foot)	A form of spastic cerebral palsy affecting only one limb
(Congenital musculoskeletal anomalies NOS) or (congenital deformity of musculoskeletal system NEC)	Congenital anomaly of musculoskeletal system
(Congenital pachyonychia) or (hypertrophic nails)	Pachyonychia congenita syndrome
(Congenital pes planus) or (flat foot: [congenital] or [rigid] or [spastic])	Congenital pes planus
(Congenital pes planus) or (flat foot: [congenital] or [rigid] or [spastic])	Rigid flat foot
(Congenital ptosis) or (blepharoptosis)	Congenital ptosis (disorder)
(Congenital renal failure) or (congenital uraemia)	Congenital renal failure
(Congenital renal failure) or (congenital uraemia)	Congenital uraemia
(Congenital respiratory anomalies NOS) or (bronchiectasis - congenital)	Congenital bronchiectasis
(Congenital respiratory anomalies NOS) or (bronchiectasis - congenital)	Congenital malformation of the respiratory system
(Congenital shortening of arm, unspecified) or (brachymelia of arm)	Reduction deformity of upper limb
(Congenital spine deformity NOS) or (congenital postural curvature of spine NOS)	Congenital postural scoliosis
(Congenital spine deformity NOS) or (congenital postural curvature of spine NOS)	Congenital kyphosis
(Congenital spine deformity NOS) or (congenital postural curvature of spine NOS)	Congenital lordosis deformity of spine (disorder)
(Congenital spine deformity NOS) or (congenital postural curvature of spine NOS)	Congenital deformity of spine
(Congenital sternomastoid torticollis) or (congenital wry neck) or (sternomastoid tumour)	Congenital torticollis
(Congenital talipes varus) or (pes varus) or (congenital clubfoot - varus)	Adductus deformity of foot
(Congenital talipes varus) or (pes varus) or (congenital clubfoot - varus)	Congenital varus deformity of foot
(Congenital toxoplasmosis (& [lymphadenopathy due to]) or (congenital hydrocephalus due to toxoplasmosis)	Lymphadenopathy due to congenital toxoplasmosis
(Congenital toxoplasmosis (& [lymphadenopathy due to]) or (congenital hydrocephalus due to toxoplasmosis)	Congenital hydrocephalus caused by toxoplasmosis
(Congenital toxoplasmosis (& [lymphadenopathy due to]) or (congenital hydrocephalus due to toxoplasmosis)	Congenital toxoplasmosis
(Congenital ureter anomaly NOS) or (ureter anomaly - congenital)	Congenital anomaly of ureter
(Congenital ureter anomaly NOS) or (ureter anomaly - congenital)	Congenital anomaly of ureter
(Congenital ureteric valves) or (occlusion of ureter)	Congenital ureteric valves
(Congenital ureteric valves) or (occlusion of ureter)	Occlusion of ureter
(Congenital) circulation: [fetal] or [system anomaly NOS (& acquired)]	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	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	Congenital absence of nose
(Congenital) or (acquired) absent thumb	Thumb absent
(Congenital) or (acquired) anomaly: [msk] or [skeletal]	Congenital anomaly of musculoskeletal system
(Congenital) or (acquired) cystic kidney disease (& [cyst] or [polycystic] or [fibrocystic] kidney)	Congenital cystic kidney disease
(Congenital) or (acquired) cystic kidney disease (& [cyst] or [polycystic] or [fibrocystic] kidney)	Congenital cystic kidney disease
(Congenital) or (acquired) diaphragm anomaly (& eventration)	Congenital anomaly of diaphragm
(Congenital) or (acquired) diaphragm anomaly (& eventration)	Congenital eventration of diaphragm
(Congenital) or (acquired) diaphragm anomaly (& eventration)	Congenital eventration of diaphragm
(Congenital) or (acquired) diaphragm anomaly (& eventration)	Congenital anomaly of diaphragm
(Congenital) or (acquired) fusion: [vulva] or [labia]	Fusion of vulva
(Congenital) or (acquired) lung cyst (& [bronchogenic])	Congenital bronchogenic cyst
(Congenital) or (acquired) palmaris et plantaris: [keratosis] or [tylosis]	Keratoderma climactericum
(Congenital) or (acquired) palmaris et plantaris: [keratosis] or [tylosis]	Hereditary diffuse palmoplantar keratoderma (disorder)
(Congenital) or (acquired) palmaris et plantaris: [keratosis] or [tylosis]	Diffuse palmoplantar keratoderma of Thost-Unna (disorder)
(Congenital) or (acquired) palmaris et plantaris: [keratosis] or [tylosis]	Keratosis
(Congenital) or (acquired) palmaris et plantaris: [keratosis] or [tylosis]	Acquired palmoplantar keratoderma (disorder)
(Congenital) or (acquired) pharyngeal pouch	Congenital diverticulum of pharynx
(Congenital) or (acquired) splenomegaly	Congenital splenomegaly
(Congenital) or (acquired) tongue: [bifid] or [fissure]	Bifid tongue
(Congenital) or (acquired) tongue: [bifid] or [fissure]	Plicated tongue
(Congenital): [macroglossia (& acquired)] or [tongue hypertrophy]	Enlargement of tongue
(Congenital): [macroglossia (& acquired)] or [tongue hypertrophy]	Congenital macroglossia
(Congenital): [macroglossia (& acquired)] or [tongue hypertrophy]	Acquired macroglossia
(Congenital: [polycystic lung] or [multiple bronchogenic cysts]) or (multiple lung cysts)	Congenital cystic lung
(Congenital: [polycystic lung] or [multiple bronchogenic cysts]) or (multiple lung cysts)	Multiple lung cysts
(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)	Congestive heart failure
(Congestive cardiac failure) or (dropsy) or (cardiac insufficiency) or (right heart failure) or (right ventricular failure)	Right ventricular failure
(Congestive cardiac failure) or (dropsy) or (cardiac insufficiency) or (right heart failure) or (right ventricular failure)	Biventricular congestive heart failure
(Congestive obstructive) or (congestive cardiomyopathy)	Congestive obstructive cardiomyopathy
(Congestive obstructive) or (congestive cardiomyopathy)	Congestive cardiomyopathy (disorder)
(Congestive obstructive) or (congestive cardiomyopathy)	Primary dilated cardiomyopathy
(Conjugate gaze) or (convergence disorders) or (other disorders of binocular eye movement)	Anomaly of vergence system
(Connection common bile duct NOS) or (pancreatectomy NEC)	Anastomosis of common bile duct
(Connection common bile duct NOS) or (pancreatectomy NEC)	Pancreatectomy
(Constitutional aplastic anaemia with malformation) or (pancytopenia - dysmelia)	Fanconi's anemia
(Constitutional aplastic anaemia with malformation) or (pancytopenia - dysmelia)	Constitutional aplastic anemia with malformation
(Construction managers) or (site agent/engineer)	Site agent/engineer
(Construction managers) or (site agent/engineer)	Site agent/engineer
(Construction managers) or (site agent/engineer)	Construction manager
(Construction managers) or (site agent/engineer)	Construction manager
(Construction worker(s)) or (builder)	Construction worker (occupation)
(Construction worker(s)) or (builder)	Builder (occupation)
(Construction worker(s)) or (builder)	Builder (occupation)
(Construction worker(s)) or (builder)	Construction worker (occupation)
(Contact dermatitis NOS) or (discoid eczema) or (nummular eczema)	Nummular eczema
(Contact dermatitis NOS) or (discoid eczema) or (nummular eczema)	Nummular eczema
(Contact dermatitis NOS) or (discoid eczema) or (nummular eczema)	Contact dermatitis

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Reference Sets

Reference set descriptor

Back to Start

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)