59229005: Familial porphyria cutanea tarda (disorder)

SNOMED CT Concept\Clinical finding\...

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

\Viscus structure finding\Abdominal organ finding\Liver finding\Liver disease\Hepatic porphyria\Porphyria cutanea tarda\Familial porphyria cutanea tarda

\Digestive system finding\Liver finding\Liver disease\Hepatic porphyria\Porphyria cutanea tarda\Familial porphyria cutanea tarda
\Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Familial porphyria cutanea tarda
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Liver disease\Hepatic porphyria\Porphyria cutanea tarda\Familial porphyria cutanea tarda

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Hepatic porphyria\Porphyria cutanea tarda\Familial porphyria cutanea tarda
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Liver finding\Liver disease\Hepatic porphyria\Porphyria cutanea tarda\Familial porphyria cutanea tarda
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Liver disease\Hepatic porphyria\Porphyria cutanea tarda\Familial porphyria cutanea tarda
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Hepatic porphyria\Porphyria cutanea tarda\Familial porphyria cutanea tarda

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

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

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

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

798048011 Familial porphyria cutanea tarda (disorder) en Fully specified name Active Case insensitive SNOMED CT core

98397018 Familial porphyria cutanea tarda en Synonym Active Case insensitive SNOMED CT core

98398011 Hereditary porphyria cutanea tarda en Synonym Active Case insensitive SNOMED CT core

98399015 PCT, type II en Synonym Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial porphyria cutanea tarda	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Familial porphyria cutanea tarda	Is a	Digestive system hereditary disorder	true	Inferred relationship	Some
Familial porphyria cutanea tarda	Is a	Hereditary disorder of the integument	true	Inferred relationship	Some
Familial porphyria cutanea tarda	Is a	Porphyria cutanea tarda	true	Inferred relationship	Some
Familial porphyria cutanea tarda	Is a	Familial disease	true	Inferred relationship	Some
Familial porphyria cutanea tarda	Occurrence	Congenital	false	Inferred relationship	Some
Familial porphyria cutanea tarda	Finding site	Skin structure	true	Inferred relationship	Some	2
Familial porphyria cutanea tarda	Finding site	Liver structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
798048011	Familial porphyria cutanea tarda (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
98397018	Familial porphyria cutanea tarda	en	Synonym	Active	Case insensitive	SNOMED CT core
98398011	Hereditary porphyria cutanea tarda	en	Synonym	Active	Case insensitive	SNOMED CT core
98399015	PCT, type II	en	Synonym	Active	Case sensitive	SNOMED CT core