238056003: Homozygous hereditary coproporphyria (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Liver finding\Liver disease\Hepatic porphyria\Hereditary coproporphyria\Homozygous hereditary coproporphyria

\Digestive system finding\Liver finding\Liver disease\Hepatic porphyria\Hereditary coproporphyria\Homozygous hereditary coproporphyria
\Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Hereditary coproporphyria\Homozygous hereditary coproporphyria
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Liver disease\Hepatic porphyria\Hereditary coproporphyria\Homozygous hereditary coproporphyria

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Hepatic porphyria\Hereditary coproporphyria\Homozygous hereditary coproporphyria
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Liver finding\Liver disease\Hepatic porphyria\Hereditary coproporphyria\Homozygous hereditary coproporphyria
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Liver disease\Hepatic porphyria\Hereditary coproporphyria\Homozygous hereditary coproporphyria
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Hepatic porphyria\Hereditary coproporphyria\Homozygous hereditary coproporphyria

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Hereditary coproporphyria\Homozygous hereditary coproporphyria
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Hereditary coproporphyria\Homozygous hereditary coproporphyria
\Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Hereditary coproporphyria\Homozygous hereditary coproporphyria
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Liver disease\Hepatic porphyria\Hereditary coproporphyria\Homozygous hereditary coproporphyria
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\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, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

356836018 Homozygous hereditary coproporphyria en Synonym Active Case insensitive SNOMED CT core

356837010 Harderoporphyria en Synonym Active Case insensitive SNOMED CT core

626885015 Homozygous hereditary coproporphyria (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Homozygous hereditary coproporphyria	Finding site	Liver structure	true	Inferred relationship	Some	1
Homozygous hereditary coproporphyria	Occurrence	Congenital	false	Inferred relationship	Some
Homozygous hereditary coproporphyria	Finding site	Pulmonary valve structure	false	Inferred relationship	Some
Homozygous hereditary coproporphyria	Finding site	Structure of skin region	false	Inferred relationship	Some
Homozygous hereditary coproporphyria	Finding site	Structure of central nervous system	false	Inferred relationship	Some
Homozygous hereditary coproporphyria	Is a	Hereditary coproporphyria	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set