238056003: Homozygous 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\Homozygous hereditary coproporphyria

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

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

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

Descriptions:

Id Description Lang Type Status Case? Module

356836018 Homozygous hereditary coproporphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

356837010 Harderoporphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626885015 Homozygous hereditary coproporphyria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Homozygous hereditary coproporphyria	localisation d'une constatation (attribut)	foie	true	Inferred relationship	Some	1
Homozygous hereditary coproporphyria	survenue (attribut)	congénital	false	Inferred relationship	Some
Homozygous hereditary coproporphyria	localisation d'une constatation (attribut)	valve pulmonaire (structure corporelle)	false	Inferred relationship	Some
Homozygous hereditary coproporphyria	localisation d'une constatation (attribut)	Structure of skin region	false	Inferred relationship	Some
Homozygous hereditary coproporphyria	localisation d'une constatation (attribut)	Structure of central nervous system (body structure)	false	Inferred relationship	Some
Homozygous hereditary coproporphyria	est un(e) (attribut)	Hereditary coproporphyria	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

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