7425008: Hereditary coproporphyria (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Liver finding\Disorder of liver\Hepatic porphyria\Hereditary coproporphyria

\Digestive system finding\Liver finding\Disorder of liver\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\Disorder of liver\Hepatic porphyria\Hereditary coproporphyria

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\Hepatic porphyria\Hereditary coproporphyria
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Liver finding\Disorder of liver\Hepatic porphyria\Hereditary coproporphyria
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of liver\Hepatic porphyria\Hereditary coproporphyria
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\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\Disorder of liver\Hepatic porphyria\Hereditary coproporphyria
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\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, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

13238015 Hereditary coproporphyria en Synonym Active Entire term case insensitive SNOMED CT core module

13239011 Berger-Goldberg syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

13240013 CPO deficiency en Synonym Active Entire term case sensitive SNOMED CT core module

13241012 CPRO deficiency en Synonym Active Entire term case sensitive SNOMED CT core module

13242017 Porphyria hepatica II en Synonym Active Only initial character case insensitive SNOMED CT core module

502646019 HCP - Hereditary coproporphyria en Synonym Active Entire term case sensitive SNOMED CT core module

502647011 Coproporphyrinogen oxidase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

502649014 CPO - Coproporphyrinogen oxidase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module

814729016 Hereditary coproporphyria (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
Hereditary coproporphyria	Is a	Multisystem disorder W-X	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Hereditary disorder of the integument	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Cardiovascular system hereditary disorder	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Heart disease	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Hereditary disorder of nervous system	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Porphyria	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Congenital anomaly of integument	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Disorder of the central nervous system	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Finding site	Structure of central nervous system	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Finding site	Pulmonary valve structure	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Finding site	Structure of skin region	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Disorder of skin	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Pulmonary valve disorder	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Multisystem disorder	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Disorder of porphyrin metabolism	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Site-specific disorder of skin	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Disorder of soft tissue of thoracic cavity	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Congenital heart disease	false	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Coproporphyria	true	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Is a	Hepatic porphyria	true	Inferred relationship	Existential restriction modifier
Hereditary coproporphyria	Finding site	Liver structure	true	Inferred relationship	Existential restriction modifier	1
Hereditary coproporphyria	Is a	Digestive system hereditary disorder	true	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Homozygous hereditary coproporphyria	Is a	True	Hereditary coproporphyria	Inferred relationship	Existential restriction modifier
Erythropoietic coproporphyria	Is a	True	Hereditary coproporphyria	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

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