61164006: Erythropoietic coproporphyria (disorder)

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

\Viscus structure finding (finding)\Abdominal organ finding\Liver finding\Disease of liver\Hepatic porphyria\Hereditary coproporphyria\Erythropoietic coproporphyria

\Digestive system finding (finding)\Liver finding\Disease of liver\Hepatic porphyria\Hereditary coproporphyria\Erythropoietic coproporphyria
\Digestive system finding (finding)\Disease of digestive system (disorder)\Digestive system hereditary disorder\Hereditary coproporphyria\Erythropoietic coproporphyria
\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\Hereditary coproporphyria\Erythropoietic coproporphyria

\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\Hereditary coproporphyria\Erythropoietic coproporphyria
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Liver finding\Disease of liver\Hepatic porphyria\Hereditary coproporphyria\Erythropoietic coproporphyria
\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\Hereditary coproporphyria\Erythropoietic coproporphyria
\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\Hereditary coproporphyria\Erythropoietic coproporphyria

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Hereditary coproporphyria\Erythropoietic coproporphyria
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Hereditary coproporphyria\Erythropoietic coproporphyria
\Disease\Disorder of body system\Disease of digestive system (disorder)\Digestive system hereditary disorder\Hereditary coproporphyria\Erythropoietic coproporphyria
\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\Hereditary coproporphyria\Erythropoietic coproporphyria
\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\Hereditary coproporphyria\Erythropoietic coproporphyria
\Disease\Metabolic disease\Disorder of porphyrin metabolism\Porphyria\Coproporphyria\Hereditary coproporphyria\Erythropoietic coproporphyria
\Disease\Metabolic disease\Disorder of porphyrin metabolism\Porphyria\Hepatic porphyria\Hereditary coproporphyria\Erythropoietic 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

101637018 Erythropoietic coproporphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

800196014 Erythropoietic coproporphyria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

101637018 Erythropoietic coproporphyria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

101637018 Erythropoietic coproporphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

800196014 Erythropoietic coproporphyria (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

800196014 Erythropoietic coproporphyria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4590671000241111 coproporphyrie érythropoïétique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4590671000241111 coproporphyrie érythropoïétique 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
Erythropoietic coproporphyria	Is a	Hereditary coproporphyria	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Erythropoietic coproporphyria	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Erythropoietic coproporphyria	Finding site	Structure of skin region (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Erythropoietic coproporphyria	Finding site	Pulmonary valve structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Erythropoietic coproporphyria	Finding site	Structure of central nervous system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Erythropoietic coproporphyria	Finding site	Liver structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets