7425008: Hereditary coproporphyria (disorder)

SNOMED CT Concept\constatation clinique\...

\Viscus structure finding (finding)\constatation à propos d'un organe abdominal\constatation à propos du foie\affection du foie\porphyrie hépatique (trouble)\Hereditary coproporphyria

\Digestive system finding (finding)\constatation à propos du foie\affection du foie\porphyrie hépatique (trouble)\Hereditary coproporphyria
\Digestive system finding (finding)\maladie de l'appareil digestif\Digestive system hereditary disorder\Hereditary coproporphyria
\Digestive system finding (finding)\maladie de l'appareil digestif\Disorder of digestive organ (disorder)\affection du foie\porphyrie hépatique (trouble)\Hereditary coproporphyria

\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\porphyrie hépatique (trouble)\Hereditary coproporphyria
\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\porphyrie hépatique (trouble)\Hereditary coproporphyria
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\affection abdominale\affection du foie\porphyrie hépatique (trouble)\Hereditary coproporphyria
\constatation à propos d'une structure du tronc\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\affection du foie\porphyrie hépatique (trouble)\Hereditary coproporphyria

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Digestive system hereditary disorder\Hereditary coproporphyria
\Disease\affection d'un système corporel\Hereditary disorder by system\Digestive system hereditary disorder\Hereditary coproporphyria
\Disease\affection d'un système corporel\maladie de l'appareil digestif\Digestive system hereditary disorder\Hereditary coproporphyria
\Disease\affection d'un système corporel\maladie de l'appareil digestif\Disorder of digestive organ (disorder)\affection du foie\porphyrie hépatique (trouble)\Hereditary coproporphyria
\Disease\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\affection du foie\porphyrie hépatique (trouble)\Hereditary coproporphyria
\Disease\trouble métabolique\Disorder of porphyrin metabolism\Porphyria (disorder)\Coproporphyria\Hereditary coproporphyria
\Disease\trouble métabolique\Disorder of porphyrin metabolism\Porphyria (disorder)\porphyrie hépatique (trouble)\Hereditary coproporphyria

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary coproporphyria	est un(e) (attribut)	affection de la peau (trouble)	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	Pulmonary valve disorder	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	Multisystem disorder (disorder)	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	Disorder of porphyrin metabolism	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	Site-specific disorder of skin	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	Disorder of soft tissue of thoracic cavity	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	maladie cardiaque congénitale	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	Multisystem disorder W-X (navigational concept)	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	Hereditary disorder of the integument	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	Congenital anomaly of trunk	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	Cardiovascular system hereditary disorder	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	cardiopathie (trouble)	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	Hereditary disorder of nervous system	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	Porphyria	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	Congenital anomaly of integument	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	Disorder of the central nervous system (disorder)	false	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	Coproporphyria	true	Inferred relationship	Some
Hereditary coproporphyria	est un(e) (attribut)	porphyrie hépatique (trouble)	true	Inferred relationship	Some
Hereditary coproporphyria	localisation d'une constatation (attribut)	foie	true	Inferred relationship	Some	1
Hereditary coproporphyria	est un(e) (attribut)	Digestive system hereditary disorder	true	Inferred relationship	Some
Hereditary coproporphyria	localisation d'une constatation (attribut)	Structure of central nervous system (body structure)	false	Inferred relationship	Some
Hereditary coproporphyria	localisation d'une constatation (attribut)	valve pulmonaire (structure corporelle)	false	Inferred relationship	Some
Hereditary coproporphyria	survenue (attribut)	congénital	false	Inferred relationship	Some
Hereditary coproporphyria	localisation d'une constatation (attribut)	Structure of skin region	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Erythropoietic coproporphyria	est un(e) (attribut)	True	Hereditary coproporphyria	Inferred relationship	Some
Homozygous hereditary coproporphyria	est un(e) (attribut)	True	Hereditary coproporphyria	Inferred relationship	Some

Reference Sets

Canada French language reference set (foundation metadata concept)

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
13238015	Hereditary coproporphyria	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
13239011	Berger-Goldberg syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
13240013	CPO deficiency	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
13241012	CPRO deficiency	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
13242017	Porphyria hepatica II	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
502646019	HCP - Hereditary coproporphyria	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
502647011	Coproporphyrinogen oxidase deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
502649014	CPO - Coproporphyrinogen oxidase deficiency	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
65991000077116	coproporphyrie héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
688111000077113	coproporphyrie héréditaire (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
814729016	Hereditary coproporphyria (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core