59229005: Familial porphyria cutanea tarda (disorder)

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

\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)

\Viscus structure finding (finding)\Abdominal organ finding\Liver finding\Disease of liver\Hepatic porphyria\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)

\Digestive system finding (finding)\Liver finding\Disease of liver\Hepatic porphyria\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)
\Digestive system finding (finding)\Disease of digestive system (disorder)\Digestive system hereditary disorder\Familial porphyria cutanea tarda (disorder)
\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\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)

\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\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Liver finding\Disease of liver\Hepatic porphyria\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)
\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\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)
\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\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)

\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument (disorder)\Familial porphyria cutanea tarda (disorder)
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Familial porphyria cutanea tarda (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Familial porphyria cutanea tarda (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial porphyria cutanea tarda (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Familial porphyria cutanea tarda (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Familial porphyria cutanea tarda (disorder)
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument (disorder)\Familial porphyria cutanea tarda (disorder)
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)
\Disease\Disorder of body system\Disease of digestive system (disorder)\Digestive system hereditary disorder\Familial porphyria cutanea tarda (disorder)
\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\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)
\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\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)
\Disease\Familial disease\Familial porphyria cutanea tarda (disorder)
\Disease\Metabolic disease\Disorder of porphyrin metabolism\Porphyria\Hepatic porphyria\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)
\Disease\Metabolic disease\Disorder of porphyrin metabolism\Uroporphyrinogen decarboxylase deficiency\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Porphyria cutanea tarda (disorder)\Familial porphyria cutanea tarda (disorder)

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
Familial porphyria cutanea tarda (disorder)	Is a	Porphyria cutanea tarda (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial porphyria cutanea tarda (disorder)	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial porphyria cutanea tarda (disorder)	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial porphyria cutanea tarda (disorder)	Finding site	Liver structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial porphyria cutanea tarda (disorder)	Is a	Familial disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial porphyria cutanea tarda (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial porphyria cutanea tarda (disorder)	Is a	Digestive system hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial porphyria cutanea tarda (disorder)	Is a	Hereditary disorder of the integument (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)

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
98397018	Familial porphyria cutanea tarda	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
98398011	Hereditary porphyria cutanea tarda	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
798048011	Familial porphyria cutanea tarda (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5247305010	PCT (porphyria cutanea tarda) type II	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
98397018	Familial porphyria cutanea tarda	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
98397018	Familial porphyria cutanea tarda	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
98398011	Hereditary porphyria cutanea tarda	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
98398011	Hereditary porphyria cutanea tarda	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
98399015	PCT, type II	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
798048011	Familial porphyria cutanea tarda (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
798048011	Familial porphyria cutanea tarda (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5247305010	PCT (porphyria cutanea tarda) type II	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
909751000172113	porphyrie cutanée tardive familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
989791000172118	porphyrie cutanée tardive type II	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
909751000172113	porphyrie cutanée tardive familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
989791000172118	porphyrie cutanée tardive type II	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module