900000000000489007: Concept inactivation indicator attribute value reference set (foundation metadata concept)

SNOMED CT Concept\SNOMED CT Model Component\Foundation metadata concept (foundation metadata concept)\Reference set\Attribute value type\Concept inactivation indicator 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
Concept inactivation indicator reference set	Is a	Attribute value type	true	Inferred relationship	Some

Members	valueId
Congenital hyperplasia	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital hyperrotation	Ambiguous
Congenital hypertrophy	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital hypertrophy of eye bulge	Ambiguous
Congenital hypodontia, multiple teeth, related to systemic disease	Ambiguous
Congenital hypodontia, multiple teeth, unrelated to systemic disease	Ambiguous
Congenital hypopigmentation	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital hypoplasia	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital hypoplasia of arch of caudal vertebra	Moved elsewhere
Congenital hypoplasia of bile duct	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital hypoplasia of claw	Moved elsewhere
Congenital hypoplasia of forepaw phalanx	Moved elsewhere
Congenital hypoplasia of hindpaw phalanx	Moved elsewhere
Congenital hypoplasia of paw	Moved elsewhere
Congenital hypoplasia of renal papilla	Ambiguous
Congenital hypoplasia of umbilical artery	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital hypothyroidism	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital hypothyroidism NOS	Limited component (foundation metadata concept)
Congenital hypothyroidism with diffuse goitre	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital hypothyroidism with diffuse goitre	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital hypothyroidism without goitre	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital hypothyroidism: [cretinism] or [NOS]	Ambiguous
Congenital hypotonia	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital ichthyosis, unspecified	Limited component (foundation metadata concept)
Congenital imperforation, high	A component that fails to comply with the current editorial guidance.
Congenital imperforation, low	A component that fails to comply with the current editorial guidance.
Congenital incomplete atrioventricular block	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital incomplete closure	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital incomplete expansion of lung	Erroneous component (foundation metadata concept)
Congenital infection: [NOS] or [cytomegalovirus] or [herpes simplex] or [toxoplasmosis]	Ambiguous
Congenital infection: [NOS] or [cytomegalovirus] or [herpes simplex] or [toxoplasmosis]	Ambiguous
Congenital insufficiency of heart valve NEC	Limited component (foundation metadata concept)
Congenital insufficiency of the pulmonary valve	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital integument anomalies (& [birthmark NOS])	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital integument anomalies (& [birthmark NOS])	Ambiguous
Congenital intestinal adhesions NOS	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital invagination	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital iodine deficiency hypothyroidism	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital iodine deficiency syndrome	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital iodine deficiency syndrome - mixed type	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital iodine deficiency syndrome - myxoedematous type	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital iodine deficiency syndrome - myxoedematous type	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital iodine deficiency syndrome - neurological type	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital keratin cyst	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital keratoconus	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital keratoderma	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital knee joint deformity NOS	Limited component (foundation metadata concept)
Congenital kyphoscoliosis	Ambiguous
Congenital kyphosis	Ambiguous
Congenital labial adhesions	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital lacrimal gland anomalies	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital laryngeal abductor palsy	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital laryngeal adductor palsy	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital laryngeal atresia	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital lateral deviation	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital lens anomaly	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital lens: [ectopic] or [displaced] or [dislocation]	Ambiguous
Congenital leukocyte adherence deficiency	Erroneous component (foundation metadata concept)
Congenital limb deformities (& [Madelung's wrist])	Ambiguous
Congenital limb deformities (& [Madelung's wrist])	Ambiguous
Congenital lip: [fistula] or [pits]	Ambiguous
Congenital lipoatrophic diabetes	Ambiguous
Congenital lipoatrophic diabetes	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital lipoatrophic diabetes	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital livedo reticularis	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital lobar emphysema	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital lobar emphysema	Ambiguous
Congenital lordosis &/or scoliosis	Ambiguous
Congenital lordosis &/or scoliosis	Ambiguous
Congenital lordosis	Erroneous component (foundation metadata concept)
Congenital lumbosacral stenosis	Moved elsewhere
Congenital luminal atresia of aortic arch	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital lymphangiectasis	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital lymphangioma	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital lymphangiomatosis	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital lymphoedema	Ambiguous
Congenital macrocolon, not aganglionic	Classification derived component
Congenital macular changes	Ambiguous
Congenital malformation	Ambiguous
Congenital malformation of genital organs	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital malformation of genital organs	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital malformation of knee	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital malformation of lacrimal gland	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital malformation of nails	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital malformation of the skin	Ambiguous
Congenital malformation of thumb	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital malformation syndrome affecting facial appearance NOS	Ambiguous
Congenital malformation syndrome associated with short stature NOS	Limited component (foundation metadata concept)
Congenital malformation syndrome due to known exogenous cause	Ambiguous
Congenital malformation syndrome involving limbs NOS	Ambiguous
Congenital malformation syndrome with metabolic disturbance NOS	Ambiguous
Congenital malformation syndrome with other skeletal changes NOS	Limited component (foundation metadata concept)
Congenital malformation syndromes affecting facial appearance	A component that is no longer current, useful, appropriate or acceptable.
Congenital malformation syndromes due to known exogenous causes	Ambiguous
Congenital malformation syndromes involving limbs	A component that is no longer current, useful, appropriate or acceptable.
Congenital malformation syndromes with metabolic disturbances	Ambiguous
Congenital malformation syndromes with other skeletal changes	Limited component (foundation metadata concept)
Congenital malocclusion	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital malposition	A component has been made inactive because it duplicates another component of the same type. E.g. A description that duplicates another description or a concept that duplicates another concept.
Congenital malposition of arch of caudal vertebra	Moved elsewhere
Congenital malposition of caudal vertebra	Moved elsewhere

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
900000000001066017	Concept inactivation indicator attribute value reference set	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)
900000000001067014	Concept inactivation indicator reference set	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)
900000000001068016	Concept inactivation indicator attribute value reference set (foundation metadata concept)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)