238057007: Homozygous variegate porphyria (disorder)

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

\Viscus structure finding (finding)\Abdominal organ finding\Liver finding\Disease of liver\Hepatic porphyria\Variegate porphyria\Homozygous variegate porphyria

\Digestive system finding (finding)\Liver finding\Disease of liver\Hepatic porphyria\Variegate porphyria\Homozygous variegate porphyria
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive organ\Disorder of liver and/or biliary tract\Disease of liver\Hepatic porphyria\Variegate porphyria\Homozygous variegate porphyria

\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\Hepatic porphyria\Variegate porphyria\Homozygous variegate porphyria
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Liver finding\Disease of liver\Hepatic porphyria\Variegate porphyria\Homozygous variegate porphyria
\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\Hepatic porphyria\Variegate porphyria\Homozygous variegate porphyria
\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\Hepatic porphyria\Variegate porphyria\Homozygous variegate porphyria

\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive organ\Disorder of liver and/or biliary tract\Disease of liver\Hepatic porphyria\Variegate porphyria\Homozygous variegate porphyria
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disorder of liver and/or biliary tract\Disease of liver\Hepatic porphyria\Variegate porphyria\Homozygous variegate porphyria
\Disease\Metabolic disease\Disorder of porphyrin metabolism\Porphyria\Hepatic porphyria\Variegate porphyria\Homozygous variegate porphyria

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

356838017 Homozygous variegate porphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626886019 Homozygous variegate porphyria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

356838017 Homozygous variegate porphyria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

356838017 Homozygous variegate porphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626886019 Homozygous variegate porphyria (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

626886019 Homozygous variegate porphyria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5021741000241117 porphyrie variegata homozygote fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5021741000241117 porphyrie variegata homozygote fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Homozygous variegate porphyria	Is a	Variegate porphyria	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Homozygous variegate porphyria	Finding site	Liver structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Homozygous variegate porphyria	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets