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. Date: 31-Jan 2002

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	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly

Members	acceptabilityId
Alcoholic drink	Acceptable (foundation metadata concept)
Alcoholic drink intake	Acceptable (foundation metadata concept)
Alcoholic fatty liver	Preferred (foundation metadata concept)
Alcoholic fatty liver (disorder)	Preferred (foundation metadata concept)
Alcoholic fatty liver disease	Acceptable (foundation metadata concept)
Alcoholic fibrosis and sclerosis of liver	Preferred (foundation metadata concept)
Alcoholic fibrosis and sclerosis of liver (disorder)	Preferred (foundation metadata concept)
Alcoholic fibrosis of liver	Acceptable (foundation metadata concept)
Alcoholic hepatic failure	Preferred (foundation metadata concept)
Alcoholic hepatic failure (disorder)	Preferred (foundation metadata concept)
Alcoholic hepatitis	Preferred (foundation metadata concept)
Alcoholic hepatitis (disorder)	Preferred (foundation metadata concept)
Alcoholic liver cirrhosis	Acceptable (foundation metadata concept)
Alcoholic liver damage	Preferred (foundation metadata concept)
Alcoholic liver damage (disorder)	Preferred (foundation metadata concept)
Alcoholic liver disease	Acceptable (foundation metadata concept)
Alcoholic steatohepatitis	Preferred (foundation metadata concept)
ALD - Alcoholic liver disease	Acceptable (foundation metadata concept)
ALF - Acute liver failure	Acceptable (foundation metadata concept)
All	Preferred (foundation metadata concept)
All postcoordinated SNOMED CT content	Preferred (foundation metadata concept)
All postcoordinated SNOMED CT content (foundation metadata concept)	Preferred (foundation metadata concept)
All precoordinated SNOMED CT content	Preferred (foundation metadata concept)
All precoordinated SNOMED CT content (foundation metadata concept)	Preferred (foundation metadata concept)
All SNOMED CT content	Preferred (foundation metadata concept)
All SNOMED CT content (foundation metadata concept)	Preferred (foundation metadata concept)
All times past	Preferred (foundation metadata concept)
All times past (qualifier value)	Preferred (foundation metadata concept)
Allergic condition	Preferred (foundation metadata concept)
Allergic condition (finding)	Preferred (foundation metadata concept)
Allergic hepatitis	Preferred (foundation metadata concept)
Allergic hepatitis (disorder)	Preferred (foundation metadata concept)
Allergic process	Preferred (foundation metadata concept)
Allergic process (qualifier value)	Preferred (foundation metadata concept)
Alpha-1-antichymotrypsin deficiency	Acceptable (foundation metadata concept)
Alpha-1-antitrypsin deficiency	Preferred (foundation metadata concept)
Alpha-1-antitrypsin deficiency (disorder)	Preferred (foundation metadata concept)
Alpha-1-antitrypsin hepatitis	Preferred (foundation metadata concept)
Alpha-1-antitrypsin hepatitis (disorder)	Preferred (foundation metadata concept)
alpha-1-Proteinase inhibitor deficiency	Acceptable (foundation metadata concept)
Alpha-methylacyl-CoA racemase deficiency disorder	Preferred (foundation metadata concept)
Alpha-methylacyl-CoA racemase deficiency disorder (disorder)	Preferred (foundation metadata concept)
Alveolar hydatid	Acceptable (foundation metadata concept)
AMACR deficiency	Acceptable (foundation metadata concept)
Amebic hepatitis	Preferred (foundation metadata concept)
Amebic hepatitis (disorder)	Preferred (foundation metadata concept)
Amebic liver abscess	Preferred (foundation metadata concept)
Amebic liver abscess (disorder)	Preferred (foundation metadata concept)
Amethopterin	Acceptable (foundation metadata concept)
Amino acid disorder	Acceptable (foundation metadata concept)
Amino acidopathy	Acceptable (foundation metadata concept)
Amiodarone	Preferred (foundation metadata concept)
Amiodarone (substance)	Preferred (foundation metadata concept)
Amniocele	Acceptable (foundation metadata concept)
Amylo-1,6-glucosidase deficiency	Acceptable (foundation metadata concept)
Amyloid	Acceptable (foundation metadata concept)
Amyloid degeneration	Acceptable (foundation metadata concept)
Amyloid deposition	Preferred (foundation metadata concept)
Amyloid deposition (morphologic abnormality)	Preferred (foundation metadata concept)
Amylopectinosis	Acceptable (foundation metadata concept)
An anatomical structure that consists of the maximal set of organ parts so connected to one another that together they constitute a self-contained unit of macroscopic anatomy, distinct both morphologically and functionally from other such units. Together with other organs, an organ constitutes an organ system or a body part. An organ is divisible into organ parts but not organs (examples: femur, biceps, liver, heart, aorta, sciatic nerve, ovary).	Preferred (foundation metadata concept)
An anomaly of bile acid synthesis with characteristics of mild cholestatic liver disease, fat malabsorption and/or neurological disease. The clinical presentation of this defect varies. Infants present with severe fat and fat-soluble vitamin deficiencies, hematochezia and mild cholestasis, whereas adults present with various neurological disorders BAS defect type 4 is caused by a mutation in the AMACR gene (5p13.2-q11.1). Transmission is autosomal recessive.	Preferred (foundation metadata concept)
An exploration using the sense of touch	Preferred (foundation metadata concept)
An immune or non-immune mediated pathological process that represents the underlying mechanism of hypersensitivity conditions.	Preferred (foundation metadata concept)
An infantile hereditary disorder of bile formation that is hepatocellular in origin and associated with extrahepatic features. Onset occurs mostly during infancy with clinical signs of cholestasis with recurrent or permanent jaundice associated with hepatomegaly and severe pruritus. Caused by mutations in the ATP8B1 gene (18q21-22) encoding the FIC1 protein expressed at the canalicular membrane of hepatocytes as well as in other epithelia. Transmission is autosomal recessive.	Preferred (foundation metadata concept)
An infusion of blood or blood product.	Preferred (foundation metadata concept)
An injection of substance or insertion of device to occlude a vessel or organ with the aim of arresting or preventing hemorrhage, blocking a lymphatic leak or devitalizing a structure or organ by occluding its blood supply.	Preferred (foundation metadata concept)
Anatomic region	Acceptable (foundation metadata concept)
Anatomical or acquired body structure	Preferred (foundation metadata concept)
Anatomical or acquired body structure (body structure)	Preferred (foundation metadata concept)
Anatomical space	Acceptable (foundation metadata concept)
Anatomical space structure	Preferred (foundation metadata concept)
Anatomical space structure (body structure)	Preferred (foundation metadata concept)
Anatomical structure	Preferred (foundation metadata concept)
Anatomical structure (body structure)	Preferred (foundation metadata concept)
Andersen disease	Acceptable (foundation metadata concept)
Andersen's disease	Acceptable (foundation metadata concept)
Angioblastoma	Acceptable (foundation metadata concept)
Angioendothelioma	Acceptable (foundation metadata concept)
Angiography of abdominal blood vessel	Preferred (foundation metadata concept)
Angiography of abdominal blood vessel (procedure)	Preferred (foundation metadata concept)
Angiography of liver	Preferred (foundation metadata concept)
Angiography of liver (procedure)	Preferred (foundation metadata concept)
Angiomyolipoma	Preferred (foundation metadata concept)
Angiomyolipoma (morphologic abnormality)	Preferred (foundation metadata concept)
Angiomyolipoma of liver	Preferred (foundation metadata concept)
Angiomyolipoma of liver (disorder)	Preferred (foundation metadata concept)
Angioplasty catheter	Preferred (foundation metadata concept)
Angioplasty catheter (physical object)	Preferred (foundation metadata concept)
Angiosarcoma	Preferred (foundation metadata concept)
Angiosarcoma (morphologic abnormality)	Preferred (foundation metadata concept)
Angiosarcoma of liver	Preferred (foundation metadata concept)
Angiosarcoma of liver (disorder)	Preferred (foundation metadata concept)
Anicteric type A viral hepatitis	Preferred (foundation metadata concept)
Anicteric type A viral hepatitis (disorder)	Preferred (foundation metadata concept)
Anicteric type B viral hepatitis	Preferred (foundation metadata concept)
Anicteric type B viral hepatitis (disorder)	Preferred (foundation metadata concept)
Anicteric viral hepatitis	Preferred (foundation metadata concept)
Anicteric viral hepatitis (disorder)	Preferred (foundation metadata concept)
Anomalous connection	Acceptable (foundation metadata concept)
Anomalous pulmonary venous drainage to hepatic veins	Preferred (foundation metadata concept)

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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)	SNOMED CT model component module (core metadata concept)
900000000001116013	US English	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component 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)	SNOMED CT model component module (core metadata concept)