238056003: Homozygous hereditary coproporphyria (disorder)

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

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

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

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

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Homozygous hereditary coproporphyria	Is a	Hereditary coproporphyria	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Homozygous hereditary coproporphyria	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Homozygous hereditary coproporphyria	Finding site	Pulmonary valve structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Homozygous hereditary coproporphyria	Finding site	Structure of skin region (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Homozygous hereditary coproporphyria	Finding site	Structure of central nervous system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Homozygous hereditary 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

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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
356836018	Homozygous hereditary coproporphyria	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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	Only initial character 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	Only initial character 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
5021721000241113	coproporphyrie héréditaire homozygote	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5021721000241113	coproporphyrie héréditaire homozygote	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module