30188007: déficit en alpha-1-antitrypsine (trouble)

SNOMED CT Concept\constatation clinique\...

\Viscus structure finding (finding)\constatation à propos d'un poumon\affection du poumon (trouble)\Alpha-1-antitrypsin deficiency (disorder)
\Viscus structure finding (finding)\constatation à propos d'un organe abdominal\constatation à propos du foie\affection du foie\troubles métaboliques et génétiques affectant le foie\Alpha-1-antitrypsin deficiency (disorder)

\Digestive system finding (finding)\constatation à propos du foie\affection du foie\troubles métaboliques et génétiques affectant le foie\Alpha-1-antitrypsin deficiency (disorder)
\Digestive system finding (finding)\maladie de l'appareil digestif\Digestive system hereditary disorder\Alpha-1-antitrypsin deficiency (disorder)
\Digestive system finding (finding)\maladie de l'appareil digestif\Disorder of digestive organ (disorder)\affection du foie\troubles métaboliques et génétiques affectant le foie\Alpha-1-antitrypsin deficiency (disorder)

\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\affection abdominale\affection du foie\troubles métaboliques et génétiques affectant le foie\Alpha-1-antitrypsin deficiency (disorder)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\constatation à propos d'un organe abdominal\constatation à propos du foie\affection du foie\troubles métaboliques et génétiques affectant le foie\Alpha-1-antitrypsin deficiency (disorder)
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\affection abdominale\affection du foie\troubles métaboliques et génétiques affectant le foie\Alpha-1-antitrypsin deficiency (disorder)
\constatation à propos d'une structure du tronc\Finding of upper trunk (finding)\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\affection du poumon (trouble)\Alpha-1-antitrypsin deficiency (disorder)
\constatation à propos d'une structure du tronc\Finding of upper trunk (finding)\Finding of region of thorax\constatation à propos d'un poumon\affection du poumon (trouble)\Alpha-1-antitrypsin deficiency (disorder)
\constatation à propos d'une structure du tronc\Finding of upper trunk (finding)\Finding of region of thorax\Disorder of thorax (disorder)\affection du poumon (trouble)\Alpha-1-antitrypsin deficiency (disorder)
\constatation à propos d'une structure du tronc\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\affection du foie\troubles métaboliques et génétiques affectant le foie\Alpha-1-antitrypsin deficiency (disorder)
\constatation à propos d'une structure du tronc\affection du tronc\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\affection du poumon (trouble)\Alpha-1-antitrypsin deficiency (disorder)

\Respiratory finding\constatation à propos des voies respiratoires inférieures\constatation à propos d'un poumon\affection du poumon (trouble)\Alpha-1-antitrypsin deficiency (disorder)
\Respiratory finding\Disorder of respiratory system (disorder)\Disorder of lower respiratory system (disorder)\affection du poumon (trouble)\Alpha-1-antitrypsin deficiency (disorder)

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Digestive system hereditary disorder\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Genetic disease\maladie héréditaire\Inborn error of metabolism\Disorder of glycoprotein metabolism\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Alpha-1-antitrypsin deficiency (disorder)
\Disease\affection d'un système corporel\Hereditary disorder by system\Digestive system hereditary disorder\Alpha-1-antitrypsin deficiency (disorder)
\Disease\affection d'un système corporel\maladie de l'appareil digestif\Digestive system hereditary disorder\Alpha-1-antitrypsin deficiency (disorder)
\Disease\affection d'un système corporel\maladie de l'appareil digestif\Disorder of digestive organ (disorder)\affection du foie\troubles métaboliques et génétiques affectant le foie\Alpha-1-antitrypsin deficiency (disorder)
\Disease\affection d'un système corporel\Disorder of respiratory system (disorder)\Disorder of lower respiratory system (disorder)\affection du poumon (trouble)\Alpha-1-antitrypsin deficiency (disorder)
\Disease\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\affection du foie\troubles métaboliques et génétiques affectant le foie\Alpha-1-antitrypsin deficiency (disorder)
\Disease\affection du tronc\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\affection du poumon (trouble)\Alpha-1-antitrypsin deficiency (disorder)
\Disease\trouble métabolique\troubles métaboliques et génétiques affectant le foie\Alpha-1-antitrypsin deficiency (disorder)
\Disease\trouble métabolique\Inborn error of metabolism\Disorder of glycoprotein metabolism\Alpha-1-antitrypsin deficiency (disorder)
\Disease\trouble métabolique\Enzymopathy\Alpha-1-antitrypsin deficiency (disorder)
\Disease\Congenital disease\Inborn error of metabolism\Disorder of glycoprotein metabolism\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)	est un(e) (attribut)	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Alpha-1-antitrypsin deficiency (disorder)	est un(e) (attribut)	Congenital anomaly of digestive system	false	Inferred relationship	Some
Alpha-1-antitrypsin deficiency (disorder)	est un(e) (attribut)	Disorder of glycoprotein metabolism	true	Inferred relationship	Some
Alpha-1-antitrypsin deficiency (disorder)	est un(e) (attribut)	Enzymopathy	true	Inferred relationship	Some
Alpha-1-antitrypsin deficiency (disorder)	est un(e) (attribut)	anomalie congénitale du poumon	false	Inferred relationship	Some
Alpha-1-antitrypsin deficiency (disorder)	est un(e) (attribut)	troubles métaboliques et génétiques affectant le foie	true	Inferred relationship	Some
Alpha-1-antitrypsin deficiency (disorder)	est un(e) (attribut)	Autosomal dominant hereditary disorder	false	Inferred relationship	Some
Alpha-1-antitrypsin deficiency (disorder)	est un(e) (attribut)	Digestive system hereditary disorder	true	Inferred relationship	Some
Alpha-1-antitrypsin deficiency (disorder)	est un(e) (attribut)	affection du poumon (trouble)	true	Inferred relationship	Some
Alpha-1-antitrypsin deficiency (disorder)	survenue (attribut)	congénital	true	Inferred relationship	Some	3
Alpha-1-antitrypsin deficiency (disorder)	localisation d'une constatation (attribut)	structure d'un poumon	true	Inferred relationship	Some	2
Alpha-1-antitrypsin deficiency (disorder)	localisation d'une constatation (attribut)	foie	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Panniculitis due to alpha-1 anti-trypsin deficiency (disorder)	Associated aetiologic finding	False	Alpha-1-antitrypsin deficiency (disorder)	Inferred relationship	Some
Alpha-1-antitrypsin hepatitis	associé à (attribut)	True	Alpha-1-antitrypsin deficiency (disorder)	Inferred relationship	Some	2
Panniculitis due to alpha-1 anti-trypsin deficiency (disorder)	Due to	True	Alpha-1-antitrypsin deficiency (disorder)	Inferred relationship	Some	2
Family history of alpha-1-antitrypsin deficiency (situation)	constatation associée (attribut)	False	Alpha-1-antitrypsin deficiency (disorder)	Inferred relationship	Some	1
Family history of alpha-1-antitrypsin deficiency (situation)	constatation associée (attribut)	True	Alpha-1-antitrypsin deficiency (disorder)	Inferred relationship	Some	1
Family history of alpha-1-antitrypsin deficiency (situation)	constatation associée (attribut)	False	Alpha-1-antitrypsin deficiency (disorder)	Inferred relationship	Some	1

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
2735705015	Alpha-1-antitrypsin deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
379101000172112	déficit en alpha-1-antitrypsine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
414911000241118	déficit en alpha-1-antitrypsine (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
484512015	Alpha-1-antitrypsin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (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