7425008: Hereditary coproporphyria (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Viscus structure finding\Abdominal organ finding\Liver finding\Liver disease\Hepatic porphyria\Hereditary coproporphyria
• \Digestive system finding\Liver finding\Liver disease\Hepatic porphyria\Hereditary coproporphyria
• \Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Hereditary coproporphyria
• \Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Liver disease\Hepatic porphyria\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
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Liver finding\Liver disease\Hepatic porphyria\Hereditary coproporphyria
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Liver disease\Hepatic porphyria\Hereditary coproporphyria
• \Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Hepatic porphyria\Hereditary coproporphyria
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Hereditary coproporphyria
• \Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Hereditary coproporphyria
• \Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Hereditary coproporphyria
• \Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Liver disease\Hepatic porphyria\Hereditary coproporphyria
• \Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Hepatic porphyria\Hereditary coproporphyria
• \Disease\Metabolic disease\Disorder of porphyrin metabolism\Porphyria\Coproporphyria\Hereditary coproporphyria
• \Disease\Metabolic disease\Disorder of porphyrin metabolism\Porphyria\Hepatic porphyria\Hereditary coproporphyria

Status: current, Defined. Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
13238015	Hereditary coproporphyria	en	Synonym	Active	Case insensitive	SNOMED CT core
13239011	Berger-Goldberg syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
13240013	CPO deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
13241012	CPRO deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
13242017	Porphyria hepatica II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
13243010	Watson syndrome	en	Synonym	Inactive	Case sensitive	SNOMED CT core
502646019	HCP - Hereditary coproporphyria	en	Synonym	Active	Case sensitive	SNOMED CT core
502647011	Coproporphyrinogen oxidase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
502648018	Watson's syndrome	en	Synonym	Inactive	Case sensitive	SNOMED CT core
502649014	CPO - Coproporphyrinogen oxidase deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
814729016	Hereditary coproporphyria (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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