30188007: Alpha-1-antitrypsin deficiency (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Viscus structure finding (finding)\Lung finding\Disease of lung (disorder)\Alpha-1-antitrypsin deficiency (disorder)
\Viscus structure finding (finding)\Abdominal organ finding\Liver finding\Disease of liver\Metabolic and genetic disorder affecting the liver\Alpha-1-antitrypsin deficiency (disorder)

\Digestive system finding (finding)\Liver finding\Disease of liver\Metabolic and genetic disorder affecting the liver\Alpha-1-antitrypsin deficiency (disorder)
\Digestive system finding (finding)\Disease of digestive system (disorder)\Digestive system hereditary disorder\Alpha-1-antitrypsin deficiency (disorder)
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive organ\Disorder of liver and/or biliary tract\Disease of liver\Metabolic and genetic disorder affecting the liver\Alpha-1-antitrypsin deficiency (disorder)
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\Alpha-1-antitrypsin deficiency (disorder)

\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disorder of liver and/or biliary tract\Disease of liver\Metabolic and genetic disorder affecting the liver\Alpha-1-antitrypsin deficiency (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Liver finding\Disease of liver\Metabolic and genetic disorder affecting the liver\Alpha-1-antitrypsin deficiency (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disease of abdomen\Disorder of liver and/or biliary tract\Disease of liver\Metabolic and genetic disorder affecting the liver\Alpha-1-antitrypsin deficiency (disorder)
\Finding of trunk structure\Finding of upper trunk (finding)\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\Disease of lung (disorder)\Alpha-1-antitrypsin deficiency (disorder)
\Finding of trunk structure\Finding of upper trunk (finding)\Finding of region of thorax\Lung finding\Disease of lung (disorder)\Alpha-1-antitrypsin deficiency (disorder)
\Finding of trunk structure\Finding of upper trunk (finding)\Finding of region of thorax\Disorder of thorax (disorder)\Disease of lung (disorder)\Alpha-1-antitrypsin deficiency (disorder)
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disorder of liver and/or biliary tract\Disease of liver\Metabolic and genetic disorder affecting the liver\Alpha-1-antitrypsin deficiency (disorder)
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\Disease of lung (disorder)\Alpha-1-antitrypsin deficiency (disorder)

\Respiratory finding\Lower respiratory tract finding\Lung finding\Disease of lung (disorder)\Alpha-1-antitrypsin deficiency (disorder)
\Respiratory finding\Disorder of respiratory system\Disease of lower respiratory system\Disease of lung (disorder)\Alpha-1-antitrypsin deficiency (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Disorder of foetus and/or newborn\Disorder of digestive system specific to fetus OR newborn\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Disorder of body system\Disease of digestive system (disorder)\Digestive system hereditary disorder\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive organ\Disorder of liver and/or biliary tract\Disease of liver\Metabolic and genetic disorder affecting the liver\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Disorder of body system\Disorder of respiratory system\Disease of lower respiratory system\Disease of lung (disorder)\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disorder of liver and/or biliary tract\Disease of liver\Metabolic and genetic disorder affecting the liver\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Disorder of trunk (disorder)\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\Disease of lung (disorder)\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Metabolic disease\Metabolic and genetic disorder affecting the liver\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Metabolic disease\Enzymopathy\Alpha-1-antitrypsin deficiency (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Alpha-1-antitrypsin deficiency (disorder)	Is a	Congenital anomaly of digestive system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha-1-antitrypsin deficiency (disorder)	Is a	Disorder of glycoprotein metabolism	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha-1-antitrypsin deficiency (disorder)	Is a	Enzymopathy	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha-1-antitrypsin deficiency (disorder)	Is a	Congenital anomaly of lung	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha-1-antitrypsin deficiency (disorder)	Is a	Metabolic and genetic disorder affecting the liver	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha-1-antitrypsin deficiency (disorder)	Is a	Autosomal dominant hereditary disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha-1-antitrypsin deficiency (disorder)	Is a	Digestive system hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha-1-antitrypsin deficiency (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Alpha-1-antitrypsin deficiency (disorder)	Finding site	Lung structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Alpha-1-antitrypsin deficiency (disorder)	Finding site	Liver structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Alpha-1-antitrypsin deficiency (disorder)	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha-1-antitrypsin deficiency (disorder)	Is a	Disease of lung (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha-1-antitrypsin deficiency (disorder)	Is a	Disorder of digestive system specific to fetus OR newborn	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Panniculitis due to alpha-1 anti-trypsin deficiency (disorder)	Associated etiologic finding	False	Alpha-1-antitrypsin deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha-1-antitrypsin hepatitis	Associated with	True	Alpha-1-antitrypsin deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Panniculitis due to alpha-1 anti-trypsin deficiency (disorder)	Due to	True	Alpha-1-antitrypsin deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Family history of alpha-1-antitrypsin deficiency	Associated finding	False	Alpha-1-antitrypsin deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Family history of alpha-1-antitrypsin deficiency	Associated finding	True	Alpha-1-antitrypsin deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Family history of alpha-1-antitrypsin deficiency	Associated finding	False	Alpha-1-antitrypsin deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	1

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
50517013	alpha-1-Proteinase inhibitor deficiency	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
484512015	Alpha-1-antitrypsin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2735705015	Alpha-1-antitrypsin deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
50516016	alpha-1-Antitrypsin deficiency	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
50517013	alpha-1-Proteinase inhibitor deficiency	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
484512015	Alpha-1-antitrypsin deficiency	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
484512015	Alpha-1-antitrypsin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
761164017	alpha-1-Antitrypsin deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
761164017	alpha-1-Antitrypsin deficiency (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2735705015	Alpha-1-antitrypsin deficiency (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2735705015	Alpha-1-antitrypsin deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
950511000195111	carenza di alfa-1-antitripsina	it	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3429491001000113	Alpha-1-Antitrypsin-Mangel	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
379101000172112	déficit en alpha-1-antitrypsine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
379101000172112	déficit en alpha-1-antitrypsine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
950511000195111	carenza di alfa-1-antitripsina	it	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3429491001000113	Alpha-1-Antitrypsin-Mangel	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module