7425008: Hereditary coproporphyria (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Viscus structure finding (finding)\Liver finding\Disease of liver\Hepatic porphyria\Hereditary coproporphyria

\Finding of trunk structure\Liver finding\Disease of liver\Hepatic porphyria\Hereditary coproporphyria
\Finding of trunk structure\Disorder of trunk (disorder)\Disease of liver\Hepatic porphyria\Hereditary coproporphyria

\Disease\Genetic disease\Hereditary disease\Hereditary coproporphyria
\Disease\Disorder of body system\Disease of liver\Hepatic porphyria\Hereditary coproporphyria
\Disease\Disorder of trunk (disorder)\Disease of liver\Hepatic porphyria\Hereditary coproporphyria
\Disease\Metabolic disease\Porphyria (disorder)\Coproporphyria\Hereditary coproporphyria
\Disease\Metabolic disease\Porphyria (disorder)\Hepatic porphyria\Hereditary coproporphyria

Status: current. Date: 31-Jul 2020

Descriptions:

Id Description Lang Type Status Case? Module

13238015 Hereditary coproporphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
13239011 Berger-Goldberg syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
13240013 CPO deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
13241012 CPRO deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
13242017 Porphyria hepatica II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
13243010 Watson syndrome en Synonym (core metadata concept) Inactive Entire term case sensitive (core metadata concept) SNOMED CT core
502646019 HCP - Hereditary coproporphyria en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
502647011 Coproporphyrinogen oxidase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
502648018 Watson's syndrome en Synonym (core metadata concept) Inactive Entire term case sensitive (core metadata concept) SNOMED CT core
502649014 CPO - Coproporphyrinogen oxidase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
814729016 Hereditary coproporphyria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary coproporphyria	Is a	Coproporphyria	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Hereditary coproporphyria	Is a	Hereditary disease	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Hereditary coproporphyria	Is a	Hepatic porphyria	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Hereditary coproporphyria	Finding site	Liver structure	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Homozygous hereditary coproporphyria	Is a	True	Hereditary coproporphyria	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Erythropoietic coproporphyria	Is a	True	Hereditary coproporphyria	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly

This concept is not in any reference sets