900000000000509007: United States of America English language reference set (foundation metadata concept)

SNOMED CT Concept\SNOMED CT Model Component\Foundation metadata concept (foundation metadata concept)\Reference set\Language type reference set (foundation metadata concept)\English [International Organization for Standardization 639-1 code en] language reference set (foundation metadata concept)\US English

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2024. Module: IPS terminology module (core metadata concept)

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
US English	Is a	English [International Organization for Standardization 639-1 code en] language reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	acceptabilityId
Congenital disorder	Acceptable (foundation metadata concept)
Congenital disorder due to abnormality of chromosome number OR structure	Acceptable (foundation metadata concept)
Congenital disorder due to abnormality of chromosome number OR structure (disorder)	Preferred (foundation metadata concept)
Congenital eye anomalies	Acceptable (foundation metadata concept)
Congenital factor IX deficiency	Acceptable (foundation metadata concept)
Congenital factor VIII deficiency	Acceptable (foundation metadata concept)
Congenital factor VIII deficiency disease	Acceptable (foundation metadata concept)
Congenital failure to descend	Acceptable (foundation metadata concept)
Congenital failure to erupt	Acceptable (foundation metadata concept)
Congenital failure to migrate	Preferred (foundation metadata concept)
Congenital failure to migrate (morphologic abnormality)	Preferred (foundation metadata concept)
Congenital familial cholemia	Acceptable (foundation metadata concept)
Congenital fissure of lip	Acceptable (foundation metadata concept)
Congenital flat foot	Acceptable (foundation metadata concept)
Congenital funnel chest	Acceptable (foundation metadata concept)
Congenital genital organ anomalies	Acceptable (foundation metadata concept)
Congenital genu valgum	Preferred (foundation metadata concept)
Congenital genu valgum (disorder)	Preferred (foundation metadata concept)
Congenital genu varum	Preferred (foundation metadata concept)
Congenital genu varum (disorder)	Preferred (foundation metadata concept)
Congenital goiter	Acceptable (foundation metadata concept)
Congenital hearing disorder	Preferred (foundation metadata concept)
Congenital hearing disorder (disorder)	Preferred (foundation metadata concept)
Congenital heart disease	Preferred (foundation metadata concept)
Congenital heart disease (disorder)	Preferred (foundation metadata concept)
Congenital hemiplegia	Acceptable (foundation metadata concept)
Congenital hepatic cyst	Acceptable (foundation metadata concept)
Congenital hydrencephalus	Acceptable (foundation metadata concept)
Congenital hydrencephaly	Acceptable (foundation metadata concept)
Congenital hydrocele	Preferred (foundation metadata concept)
Congenital hydrocele (disorder)	Preferred (foundation metadata concept)
Congenital hydrocele of tunica vaginalis	Acceptable (foundation metadata concept)
Congenital hydrocephalus	Preferred (foundation metadata concept)
Congenital hydrocephalus (disorder)	Preferred (foundation metadata concept)
Congenital hydrocephaly	Acceptable (foundation metadata concept)
Congenital hyperplasia of retinal pigment epithelium	Acceptable (foundation metadata concept)
Congenital hypertrophy of retinal pigment epithelium	Preferred (foundation metadata concept)
Congenital hypertrophy of retinal pigment epithelium (disorder)	Preferred (foundation metadata concept)
Congenital hypothyroidism not due to iodine deficiency	Acceptable (foundation metadata concept)
Congenital hypotonia	Acceptable (foundation metadata concept)
Congenital incomplete expansion	Preferred (foundation metadata concept)
Congenital incomplete expansion (morphologic abnormality)	Preferred (foundation metadata concept)
Congenital incomplete inflation	Acceptable (foundation metadata concept)
Congenital infection	Acceptable (foundation metadata concept)
Congenital infectious disease	Preferred (foundation metadata concept)
Congenital infectious disease (disorder)	Preferred (foundation metadata concept)
Congenital insufficiency of tricuspid valve	Preferred (foundation metadata concept)
Congenital insufficiency of tricuspid valve (disorder)	Preferred (foundation metadata concept)
Congenital iodine deficiency syndrome	Preferred (foundation metadata concept)
Congenital iodine deficiency syndrome (disorder)	Preferred (foundation metadata concept)
Congenital knock-knee	Acceptable (foundation metadata concept)
Congenital kyphoscoliosis	Preferred (foundation metadata concept)
Congenital kyphoscoliosis (disorder)	Preferred (foundation metadata concept)
Congenital laryngomalacia	Preferred (foundation metadata concept)
Congenital laryngomalacia (disorder)	Preferred (foundation metadata concept)
Congenital lesion of nervous system	Acceptable (foundation metadata concept)
Congenital lumbosacral spondylolysis	Acceptable (foundation metadata concept)
Congenital macrocephaly	Preferred (foundation metadata concept)
Congenital macrocephaly (disorder)	Preferred (foundation metadata concept)
Congenital malformation	Preferred (foundation metadata concept)
Congenital malformation (disorder)	Preferred (foundation metadata concept)
Congenital malformation of eye	Acceptable (foundation metadata concept)
Congenital malformation of genital organs	Preferred (foundation metadata concept)
Congenital malformation of genital organs (disorder)	Preferred (foundation metadata concept)
Congenital malformation of lips	Acceptable (foundation metadata concept)
Congenital malformation of mouth	Acceptable (foundation metadata concept)
Congenital malformation of spine	Acceptable (foundation metadata concept)
Congenital malformation of the digestive system	Acceptable (foundation metadata concept)
Congenital malformation of the esophagus	Acceptable (foundation metadata concept)
Congenital malformation of the nervous system	Acceptable (foundation metadata concept)
Congenital malformation of the skin	Acceptable (foundation metadata concept)
Congenital malformation of upper alimentary tract	Preferred (foundation metadata concept)
Congenital malformation of upper alimentary tract (disorder)	Preferred (foundation metadata concept)
Congenital malformation syndrome	Preferred (foundation metadata concept)
Congenital malformation syndrome (disorder)	Preferred (foundation metadata concept)
Congenital melanocytic nevus	Preferred (foundation metadata concept)
Congenital melanocytic nevus	Acceptable (foundation metadata concept)
Congenital melanocytic nevus (morphologic abnormality)	Preferred (foundation metadata concept)
Congenital metatarsus adductus	Acceptable (foundation metadata concept)
Congenital metatarsus varus	Acceptable (foundation metadata concept)
Congenital microcephalus	Acceptable (foundation metadata concept)
Congenital microcephaly	Preferred (foundation metadata concept)
Congenital microcephaly (disorder)	Preferred (foundation metadata concept)
Congenital narrowed aorta	Acceptable (foundation metadata concept)
Congenital nasal septum deviation	Acceptable (foundation metadata concept)
Congenital nasolacrimal duct obstruction	Preferred (foundation metadata concept)
Congenital nasolacrimal duct obstruction (disorder)	Preferred (foundation metadata concept)
Congenital nystagmus	Preferred (foundation metadata concept)
Congenital nystagmus (disorder)	Preferred (foundation metadata concept)
Congenital obstruction of lacrimal canal	Preferred (foundation metadata concept)
Congenital obstruction of lacrimal canaliculus	Acceptable (foundation metadata concept)
Congenital obstruction of lacrimal canaliculus (disorder)	Preferred (foundation metadata concept)
Congenital obstruction of ureteropelvic junction	Preferred (foundation metadata concept)
Congenital obstruction of ureteropelvic junction (disorder)	Preferred (foundation metadata concept)
Congenital omphalocele	Preferred (foundation metadata concept)
Congenital omphalocele (disorder)	Preferred (foundation metadata concept)
Congenital ossification of cranial sutures	Acceptable (foundation metadata concept)
Congenital ossification of sutures of skull	Acceptable (foundation metadata concept)
Congenital osteopetrosis	Acceptable (foundation metadata concept)
Congenital pectus excavatum	Preferred (foundation metadata concept)
Congenital pectus excavatum (disorder)	Preferred (foundation metadata concept)

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
900000000001115012	United States of America English language reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	IPS terminology module (core metadata concept)
900000000001116013	US English	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	IPS terminology module (core metadata concept)
900000000001117016	United States of America English language reference set (foundation metadata concept)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	IPS terminology module (core metadata concept)