61860000: Porphyria cutanea tarda (disorder)

SNOMED CT Concept\Clinical finding\...

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

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

\Digestive system finding\Liver finding\Disorder of liver\Hepatic porphyria\Porphyria cutanea tarda
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Disorder of liver\Hepatic porphyria\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
\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
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of liver\Hepatic porphyria\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

\General finding of soft tissue\Skin finding\Disorder of skin\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

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

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

102819015 Porphyria cutanea tarda en Synonym Active Entire term case insensitive SNOMED CT core module

102821013 Symptomatic porphyria en Synonym Active Entire term case insensitive SNOMED CT core module

102822018 Cutaneous hepatic porphyria en Synonym Active Entire term case insensitive SNOMED CT core module

102823011 PCT en Synonym Active Entire term case sensitive SNOMED CT core module

102824017 Porphyria cutanea tarda symptomatica en Synonym Active Entire term case insensitive SNOMED CT core module

102825016 Porphyria, hepatocutaneous type en Synonym Active Entire term case insensitive SNOMED CT core module

102826015 Urocoproporphyria en Synonym Active Entire term case insensitive SNOMED CT core module

102827012 UROD deficiency en Synonym Active Entire term case sensitive SNOMED CT core module

499144011 PCT - Porphyria cutanea tarda en Synonym Active Entire term case sensitive SNOMED CT core module

499145012 CHP - Cutaneous hepatic porphyria en Synonym Active Entire term case sensitive SNOMED CT core module

800968016 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
Porphyria cutanea tarda	Is a	Hereditary disorder of the integument	false	Inferred relationship	Existential restriction modifier
Porphyria cutanea tarda	Is a	Congenital anomaly of integument	false	Inferred relationship	Existential restriction modifier
Porphyria cutanea tarda	Is a	Hepatic porphyria	true	Inferred relationship	Existential restriction modifier
Porphyria cutanea tarda	Is a	Uroporphyrinogen decarboxylase deficiency	true	Inferred relationship	Existential restriction modifier
Porphyria cutanea tarda	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	2
Porphyria cutanea tarda	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Porphyria cutanea tarda	Finding site	Liver structure	true	Inferred relationship	Existential restriction modifier	1
Porphyria cutanea tarda	Is a	Disorder of skin	true	Inferred relationship	Existential restriction modifier
Porphyria cutanea tarda	Is a	Disorder of soft tissue of body cavity	false	Inferred relationship	Existential restriction modifier
Porphyria cutanea tarda	Is a	Disorder of soft tissue of body cavity	false	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Homozygous porphyria cutanea tarda	Is a	True	Porphyria cutanea tarda	Inferred relationship	Existential restriction modifier
Familial porphyria cutanea tarda	Is a	True	Porphyria cutanea tarda	Inferred relationship	Existential restriction modifier
Sporadic porphyria cutanea tarda	Is a	True	Porphyria cutanea tarda	Inferred relationship	Existential restriction modifier
Neonatal jaundice with porphyria	Associated with	False	Porphyria cutanea tarda	Inferred relationship	Existential restriction modifier
Acquired porphyria cutanea tarda	Is a	True	Porphyria cutanea tarda	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets