900000000000527005: SAME AS 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)\SAME AS 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

900000000001158011 SAME AS 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)

900000000001159015 SAME AS 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
SAME AS association reference set (foundation metadata concept)	Is a	Historical association reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	targetComponentId
Congenital hydronephrosis	Congenital hydronephrosis
Congenital hyperpigmentation	Hyperpigmentation
Congenital hyperplasia	Hyperplasia
hypertrophie congénitale	Hypertrophy
Congenital hypopigmentation	Hypopigmentation
Congenital hypoplasia	Hypoplasia
Congenital hypoplasia of bile duct	Congenital hypoplasia of bile duct
Congenital hypoplasia of umbilical artery	Congenital hypoplasia of umbilical artery
Congenital hypothyroidism	Endemic cretinism
Congenital hypothyroidism with diffuse goitre	Congenital hypothyroidism with diffuse goitre
Congenital hypothyroidism with diffuse goitre	Congenital hypothyroidism with diffuse goitre
Congenital hypothyroidism without goitre	Congenital hypothyroidism without goitre
Congenital hypotonia	Neonatal hypotonia
Congenital incomplete atrioventricular block	Congenital incomplete atrioventricular heart block
Congenital incomplete closure	Developmental failure of fusion (morphologic abnormality)
Congenital insufficiency of the pulmonary valve	Congenital insufficiency of pulmonary valve
Congenital integument anomalies (& [birthmark NOS])	Congenital anomaly of integument
Congenital intestinal adhesions NOS	Adhesion
Congenital invagination	Invagination
Congenital iodine deficiency hypothyroidism	Endemic cretinism
Congenital iodine deficiency syndrome	Endemic cretinism
Congenital iodine deficiency syndrome - mixed type	Congenital iodine deficiency syndrome of mixed type (disorder)
Congenital iodine deficiency syndrome - myxoedematous type	Endemic cretinism
Congenital iodine deficiency syndrome - myxoedematous type	Endemic cretinism
Congenital iodine deficiency syndrome - neurological type	Congenital iodine deficiency syndrome of neurological type (disorder)
Congenital keratin cyst	Keratinizing cyst (morphologic abnormality)
Congenital keratoconus	Congenital keratoconus (disorder)
Congenital keratoderma	Congenital keratoderma
Congenital labial adhesions	Congenital labial adhesion
Congenital lacrimal gland anomalies	Congenital anomaly of lacrimal gland
Congenital laryngeal abductor palsy	Congenital laryngeal abductor palsy
Congenital laryngeal adductor palsy	Congenital laryngeal adductor palsy (disorder)
Congenital laryngeal atresia	Congenital atresia of larynx
Congenital lateral deviation	Lateral displacement
Congenital lens anomaly	Congenital anomaly of lens
Congenital lipoatrophic diabetes	Congenital total lipodystrophy (disorder)
Congenital lipoatrophic diabetes	Congenital total lipodystrophy (disorder)
Congenital livedo reticularis	Congenital livedo reticularis
Congenital lobar emphysema	Congenital emphysema (disorder)
Congenital luminal atresia of aortic arch	Congenital atresia of aortic arch (disorder)
Congenital lymphangiectasis	Lymphangiectasis
Congenital lymphangioma	Congenital lymphangioma
Congenital lymphangiomatosis	Lymphangiomatosis
Congenital malformation of genital organs	Congenital malformation of genital organs
Congenital malformation of genital organs	Congenital malformation of genital organs
Congenital malformation of knee	Congenital deformity of knee joint
Congenital malformation of lacrimal gland	Congenital anomaly of lacrimal system
Congenital malformation of nails	Congenital anomaly of nail
Congenital malformation of thumb	Congenital malformation of thumb (disorder)
Congenital malocclusion	Malocclusion (morphologic abnormality)
Congenital malposition	Malposition (morphologic abnormality)
Congenital malposition, complete	Malposition (morphologic abnormality)
Congenital malposition, multiple	Malposition (morphologic abnormality)
Congenital malposition, partial	Malposition (morphologic abnormality)
Congenital mandibular hypoplasia	Congenital micrognathism
Congenital megacolon	Congenital dilatation of colon
Congenital megaloureter	Congenital dilatation of ureter (disorder)
Congenital melanocytic nevus of skin	Congenital pigmented melanocytic nevus of skin (disorder)
Congenital mitral regurgitation	Congenital insufficiency of mitral valve
Congenital morphological disturbances of hair	Congenital anomaly of hair
Congenital myotonia	A rare, genetic, skeletal muscle channelopathy characterized by slow muscle relaxation after contraction (myotonia).
Congenital nasal deformity	Congenital deformity of nose (disorder)
Congenital neutropenia	Congenital neutropenia
Congenital non-obstructive megaureter	Dilatation of ureter
Congenital non-progressive ataxia	Congenital non-progressive ataxia
Congenital notching of palpebral fissure	Coloboma of eyelid
Congenital notching of tip of nose	Congenital notching of tip of nose
Congenital nystagmus	Congenital nystagmus
Congenital obstruction	Obstruction
Congenital obstruction of large intestine	Congenital obstruction of large intestine
Congenital obstruction of small intestine	Congenital obstruction of small intestine
Congenital obstruction of urethra	Congenital obstruction of urethra
Congenital occlusion of anus	Congenital occlusion of anus
Congenital oesophageal web	Congenital web of esophagus
Congenital omphalocele	Congenital omphalocele
Congenital onychauxis	Congenital onychauxis
Congenital opacity	Abnormally opaque structure (morphologic abnormality)
Congenital opacity of vitreous body	Congenital vitreous opacity
Congenital optic disc anomaly	Congenital anomaly of optic disc
Congenital optic disc anomaly	Congenital anomaly of optic disc
Congenital optic disc anomaly	Congenital anomaly of optic disc
Congenital optic disc coloboma	Congenital coloboma of optic disc
Congenital optic disc coloboma	Congenital coloboma of optic disc
anomalie vaginale congénitale ou acquise dans le cadre d'une grossesse, d'un accouchement et d'un postpartum	Vaginal abnormality in pregnancy, childbirth and the puerperium
Congenital orbit anomalies	Congenital structural abnormality of orbit proper (disorder)
Congenital ovarian dysplasia	Congenital ovarian dysplasia
Congenital partial hypoplasia	Hypoplasia
Congenital partial opacity	Abnormally opaque structure (morphologic abnormality)
Congenital perforation	Perforation
Congenital perforation of wall of nasal sinus	Congenital perforation of the nasal sinus wall
Congenital pes planus	Congenital pes planus
Congenital pigmentary anomaly of skin	Congenital pigmentary skin anomalies
Congenital pigmentation	Pigment deposition
Congenital pneumonia	Congenital pneumonia
Congenital polycystic lung	Congenital cystic lung
Portosystemischer Shunt, kongenitaler	Congenital portal-systemic shunt
Congenital positional talipes	Congenital positional talipes (disorder)
Congenital posterior cleft of cricoid cartilage	Congenital cleft of posterior cricoid cartilage
Congenital posterior urethral valves	Congenital posterior urethral valves
Congenital posterior urethral valves	Congenital posterior urethral valves
Congenital preauricular fistula	Preauricular fistula

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
900000000001158011	SAME AS 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)
900000000001159015	SAME AS association reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)