61164006: Erythropoietic coproporphyria (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Viscus structure finding (finding)\Liver finding\Disease of liver\Hepatic porphyria\Hereditary coproporphyria\Erythropoietic coproporphyria
• \Finding of trunk structure\Liver finding\Disease of liver\Hepatic porphyria\Hereditary coproporphyria\Erythropoietic coproporphyria
• \Finding of trunk structure\Disorder of trunk (disorder)\Disease of liver\Hepatic porphyria\Hereditary coproporphyria\Erythropoietic coproporphyria
• \Disease\Genetic disease\Hereditary disease\Hereditary coproporphyria\Erythropoietic coproporphyria
• \Disease\Disorder of body system\Disease of liver\Hepatic porphyria\Hereditary coproporphyria\Erythropoietic coproporphyria
• \Disease\Disorder of trunk (disorder)\Disease of liver\Hepatic porphyria\Hereditary coproporphyria\Erythropoietic coproporphyria
• \Disease\Metabolic disease\Porphyria (disorder)\Coproporphyria\Hereditary coproporphyria\Erythropoietic coproporphyria
• \Disease\Metabolic disease\Porphyria (disorder)\Hepatic porphyria\Hereditary coproporphyria\Erythropoietic coproporphyria

Status: current. Date: 31-Jan 2002

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
101637018	Erythropoietic coproporphyria	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
800196014	Erythropoietic coproporphyria (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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