111386004: Homozygous porphyria cutanea tarda (disorder)

SNOMED CT Concept\Clinical finding\...

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

\Viscus structure finding\Abdominal organ finding\Liver finding\Disorder of liver\Hepatic porphyria\Porphyria cutanea tarda\Homozygous porphyria cutanea tarda

\Digestive system finding\Liver finding\Disorder of liver\Hepatic porphyria\Porphyria cutanea tarda\Homozygous porphyria cutanea tarda
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Disorder of liver\Hepatic porphyria\Porphyria cutanea tarda\Homozygous porphyria cutanea tarda

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

\General finding of soft tissue\Skin finding\Disorder of skin\Porphyria cutanea tarda\Homozygous 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\Homozygous porphyria cutanea tarda

\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Porphyria cutanea tarda\Homozygous porphyria cutanea tarda
\Integumentary system finding\Skin finding\Disorder of skin\Porphyria cutanea tarda\Homozygous porphyria cutanea tarda

\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Porphyria cutanea tarda\Homozygous porphyria cutanea tarda
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Disorder of liver\Hepatic porphyria\Porphyria cutanea tarda\Homozygous porphyria cutanea tarda
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\Hepatic porphyria\Porphyria cutanea tarda\Homozygous porphyria cutanea tarda
\Disease\Metabolic disease\Disorder of porphyrin metabolism\Porphyria\Hepatic porphyria\Porphyria cutanea tarda\Homozygous porphyria cutanea tarda
\Disease\Metabolic disease\Disorder of porphyrin metabolism\Uroporphyrinogen decarboxylase deficiency\Porphyria cutanea tarda\Homozygous porphyria cutanea tarda
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Porphyria cutanea tarda\Homozygous porphyria cutanea tarda

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

178624018 Homozygous porphyria cutanea tarda en Synonym Active Entire term case insensitive SNOMED CT core module
187767010 Hepatoerythropoietic porphyria en Synonym Active Entire term case insensitive SNOMED CT core module
630960010 Homozygous porphyria cutanea tarda (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Homozygous porphyria cutanea tarda	Is a	Porphyria cutanea tarda	true	Inferred relationship	Existential restriction modifier
Homozygous porphyria cutanea tarda	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Homozygous porphyria cutanea tarda	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	2
Homozygous porphyria cutanea tarda	Finding site	Liver structure	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets