900000000000528000: WAS A 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)\WAS A association reference set

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:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
WAS A association reference set	Is a	Historical association reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	targetComponentId
Conduction disorders NOS	Conduction disorder of the heart
Conduction disorders unspecified	Conduction disorder of the heart
Conductive hearing loss NOS	Conductive hearing loss
Cone biopsy of cervix uteri NEC	Cone biopsy of cervix
Cone biopsy of cervix uteri NEC	Cone biopsy of cervix
Confidential data NOS	Confidential patient data held
Confidential data NOS	Confidential patient data held
Conflagration in other building or structure	Accident caused by fire and flames
Conflagration not in building or structure NOS	Conflagration not in building or structure
Congenital CNS anomalies NOS	Congenital anomaly of nervous system
Congenital CNS anomalies NOS	Congenital anomaly of nervous system
Congenital CNS anomalies NOS	Congenital anomaly of nervous system
Congenital CVS anomaly NOS	Congenital anomaly of cardiovascular system
Congenital CVS anomaly NOS	Congenital anomaly of cardiovascular system
Congenital CVS anomaly NOS	Congenital anomaly of cardiovascular system
Congenital abnormality of uterus in pregnancy, childbirth or the puerperium NOS	Congenital abnormality of uterus in pregnancy, childbirth and the puerperium
Congenital absence finger NOS	Congenital absence of all fingers
Congenital absence of digestive system NOS	Congenital anomaly of digestive system
Congenital absence of digits NOS	Adactyly
Congenital absence of external ear, unspecified	Congenital absence of external ear
Congenital absence of kidney NOS	Renal agenesis
Congenital absence of limb NOS	Longitudinal deficiency of limb
Congenital absence of muscle or tendon NOS	Congenital absence of muscle AND/OR tendon
Congenital absence of nose NOS	Congenital absence of nose
Congenital absence of other lesser toe	Congenital absence of toe
Congenital absence of other multiple toes	Congenital absence of multiple toes
Congenital absence of pubis NEC	Congenital absence of pubis
Congenital absence of spine NEC	Congenital absence of spine
Congenital absence of vertebra NOS	Congenital absence of vertebra
Congenital adrenal hyperplasia NEC	Congenital adrenal hyperplasia
Congenital agranulocytosis NEC	Congenital neutropenia
Congenital alopecia NOS	Congenital localised alopecia
Congenital alopecia, unspecified	Congenital alopecia
Congenital amputation of unspecified limb	Congenital anomaly of limb
Congenital aneurysm NEC	Congenital arterial aneurysm
Congenital anomalies of cervical vertebrae NEC	Congenital anomaly of spine
Congenital anomalies of foot NEC	Congenital abnormality of foot and toes (disorder)
Congenital anomalies of lumbar vertebrae NEC	Congenital anomaly of spine
Congenital anomalies of ovaries NOS	Congenital anomaly of ovary
Congenital anomalies of posterior segment NOS	Congenital anomaly of posterior segment of eye
Congenital anomalies of thoracic vertebrae NEC	Congenital anomaly of spine
Congenital anomaly NOS	Congenital disease (disorder)
Congenital anomaly NOS	Congenital disease (disorder)
Congenital anomaly NOS	Congenital disease (disorder)
Congenital anomaly NOS	Congenital disease (disorder)
Congenital anomaly of cervical vertebrae NEC NOS	Congenital anomaly of spine
Congenital anomaly of face NOS	Congenital disease (disorder)
Congenital anomaly of lacrimal passages NOS	Congenital abnormality of lacrimal drainage system (disorder)
Congenital anomaly of lumbar vertebra NEC NOS	Congenital anomaly of spine
Congenital anomaly of neck NOS	Congenital anomaly of neck
Congenital anomaly of thoracic vertebrae NEC NOS	Congenital anomaly of spine
Congenital anomaly of unspecified limb NOS	Congenital anomaly of limb
Congenital anomaly: [upper GIT NOS] or [oesophagus]	Congenital malformation of upper alimentary tract
Congenital aortic valve insufficiency NOS	Congenital insufficiency of aortic valve
Congenital aortic valve insufficiency, unspecified	Congenital insufficiency of aortic valve
Congenital aplasia of genital organ NEC	Congenital malformation of genital organs (disorder)
Congenital aplasia of genital organ NEC NOS	Congenital malformation of genital organs (disorder)
Congenital atresia of pulmonary valve NOS	Congenital atresia of the pulmonary valve (disorder)
Congenital bladder neck obstruction NOS	Congenital obstruction of bladder neck
Congenital bowing of long leg bone, unspecified	Congenital leg bone bowing
Congenital brain aneurysm NEC	Congenital arterial aneurysm
Congenital cardiovascular disorder - unspecified whether during pregnancy or the puerperium	Congenital cardiovascular disorders during pregnancy, childbirth and the puerperium
Congenital cardiovascular disorder during pregnancy, childbirth or the puerperium NOS	Congenital cardiovascular disorders during pregnancy, childbirth and the puerperium
Congenital cataract or lens anomaly NOS	Congenital anomaly of lens (disorder)
Congenital cataract, unspecified	Congenital cataract
Congenital cerebral cyst NOS	Congenital cerebral cyst
Congenital cerebral palsy NOS	Cerebral palsy
Congenital cerebral palsy NOS	Cerebral palsy
Congenital corneal opacities NOS	Congenital corneal opacity
Congenital cystic kidney disease NOS	Congenital cystic kidney disease
Congenital cystic liver disease NOS	Congenital cystic disease of liver
Congenital cystic lung NOS	Congenital cystic lung
Congenital cystic lung disease, unspecified	Congenital cystic lung
Congenital deficiency of other clotting factor NOS	Blood coagulation disorder
Congenital deficiency of other clotting factors	Blood coagulation disorder
Congenital deformity of musculoskeletal system NEC	Congenital anomaly of musculoskeletal system
Congenital deformity of scapula NEC	Congenital anomaly of upper limb
Congenital diplegia NOS	Diplegic cerebral palsy
Congenital dislocation of hip NOS	Congenital dislocation of hip
Congenital dislocation of hip NOS	Congenital dislocation of hip
Congenital dislocation of one hip with subluxation of other hip	Congenital deformity of hip joint
Congenital dyserythropoiesis NEC	Congenital dyserythropoietic anemia
Congenital ear anomaly NOS	Congenital malformation of ear
Congenital esophageal fistula NOS	Congenital oesophageal fistula
Congenital eye anomalies NOS	Congenital anomaly of eye
Congenital eyelid deformity NOS	Congenital anomaly of eyelid
Congenital folds or cysts of the posterior segment NOS	Congenital fold and cyst of posterior segment of eye (disorder)
Congenital giant colon NEC	Congenital functional disorders of the colon
Congenital heart block NOS	Complete atrioventricular block
Congenital heart block, unspecified	Complete atrioventricular block
Congenital hereditary muscular dystrophy NOS	Muscular dystrophy
Congenital hydrocephalus NOS	Congenital hydrocephalus
Congenital hyperbilirubinemia NOS	Disorders of bilirubin excretion
Congenital hypothyroidism NOS	Congenital hypothyroidism
Congenital ichthyosis, unspecified	Congenital ichthyosis of skin
Congenital insufficiency of heart valve NEC	Congenital heart disease
Congenital knee joint deformity NOS	Congenital deformity of knee joint
Congenital malformation syndrome associated with short stature NOS	Congenital malformation syndromes associated with short stature
Congenital malformation syndrome with other skeletal changes NOS	Congenital malformation syndrome (disorder)
Congenital malformation syndrome with other skeletal changes NOS	Congenital anomaly of musculoskeletal system
Congenital malformation syndromes with other skeletal changes	Congenital malformation syndrome (disorder)

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
900000000001160013	WAS A association reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)
900000000001161012	WAS A 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)
7484821000172114	referentieset voor associaties betreffende voormalige ouderconcepten	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
7484831000172112	referentieset voor vroegere supertypen	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)