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403832004: Inherited disorder of porphyrin metabolism (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1771758010 Inherited disorder of porphyrin metabolism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1782836013 Inherited disorder of porphyrin metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1771758010 Inherited disorder of porphyrin metabolism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1771758010 Inherited disorder of porphyrin metabolism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1782836013 Inherited disorder of porphyrin metabolism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1782836013 Inherited disorder of porphyrin metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5264941000241118 affection héréditaire du métabolisme des porphyrines fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5264941000241118 affection héréditaire du métabolisme des porphyrines fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

12 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Inherited disorder of porphyrin metabolism (disorder) Is a Disorder of porphyrin metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Inherited disorder of porphyrin metabolism (disorder) Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Inherited disorder of porphyrin metabolism (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Inherited disorder of porphyrin metabolism (disorder) Is a Hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
Inherited disorder of porphyrin metabolism (disorder) Is a Hereditary metabolic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary sideroblastic anemia Is a False Inherited disorder of porphyrin metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital porphyria Is a True Inherited disorder of porphyrin metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
X-linked sideroblastic anaemia with spinocerebellar ataxia Is a False Inherited disorder of porphyrin metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A constitutional microcytic, hypochromic anemia of varying severity that is clinically characterized by manifestations of anemia and iron overload and that may respond to treatment with pyridoxine and folic acid. Is a True Inherited disorder of porphyrin metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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