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 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 metatarsus adductus of bilateral feet	Bilateral metatarsus varus
Congenital mitral regurgitation	Congenital insufficiency of mitral valve
Congenital morphological disturbances of hair	Congenital anomaly of hair
Congenital nasal deformity	Congenital deformity of nose
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	Opacity
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
Congenital or acquired abnormality of vagina in pregnancy, childbirth and the puerperium	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	Opacity
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
Congenital portosystemic shunt	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
Congenital precerebral nonruptured aneurysm	Congenital aneurysm of precerebral artery (disorder)
Congenital prolapse	Prolapse (morphologic abnormality)
Congenital prolapse of uterus	Congenital prolapsed uterus
Congenital protrusion	Protrusion
Congenital ptosis	Congenital ptosis (disorder)
Congenital ptosis of upper eyelid	Congenital ptosis (disorder)
Congenital pulmonary valve stenosis	Congenital stenosis of pulmonary valve
Congenital pure red cell aplasia	Congenital hypoplastic anemia
Congenital pyloric hypertrophy	Congenital hypertrophy of pylorus
Congenital pyloric spasm	Congenital pyloric spasm
Congenital pyloric stenosis	Congenital pyloric stenosis
Congenital rectourethral fistula	Congenital urethrorectal fistula
Congenital renal dysplasia	Renal dysplasia
Congenital retinal aneurysm	Congenital retinal aneurysm
Congenital rubella syndrome	Congenital rubella syndrome
Congenital scar	Congenital scar
Congenital scoliosis	Congenital postural scoliosis
Congenital short Achilles tendon	Congenital short Achilles tendon
Congenital shortening of leg	Longitudinal deficiency of lower limb
Congenital shortening of upper limb	Longitudinal deficiency of upper limb
Congenital spade-like hand	Congenital spade-like hand
Congenital spinal cord anomaly	Congenital anomaly of spinal cord (disorder)
Congenital spinal hydromeningocele	Congenital spinal meningocele
Congenital splenomegaly	Congenital splenomegaly
Congenital stenosis	Stenosis (morphologic abnormality)
Congenital stenosis of external auditory canal	Congenital stenosis of external auditory canal
Congenital sternomastoid torticollis	Congenital torticollis
Congenital stricture of oesophagus	Congenital oesophageal ring
Congenital stricture of rectum	Congenital stricture of rectum
Congenital subluxation of left hip	Congenital subluxation of left hip joint
Congenital subluxation of right hip	Congenital subluxation of right hip joint
Congenital syphilis	Congenital syphilis
Congenital syphilitic coryza	Congenital syphilitic rhinitis
Congenital syphilitic epiphysitis	Congenital syphilitic osteochondritis
Congenital syphilitic gumma	Congenital syphilis with gumma
Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Congenital syphilitic meningitis	Congenital syphilitic meningitis
Congenital syphilitic osteochondritis	Congenital syphilitic osteochondritis
Congenital syphilitic pemphigus	Congenital syphilitic pemphigus
Congenital syphilitic periostitis	Congenital syphilitic periostitis
Congenital syphilitic splenomegaly	Congenital syphilitic splenomegaly
Congenital talipes calcaneus	Congenital talipes calcaneus
Congenital talipes equinovalgus	Talipes equinovalgus
Congenital telangiectasis	Telangiectasis
Congenital thrombocytopenia	Congenital thrombocytopenia (disorder)
Congenital torsion of ovary	Congenital torsion of ovary

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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)