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276265003: Ferrochelatase deficiency (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
412335012 Ferrochelatase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
412336013 FECH - Ferrochelatase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
669159017 Ferrochelatase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

5 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ferrochelatase deficiency Is a Disorder of porphyrin and heme metabolism false Inferred relationship Existential restriction modifier
Ferrochelatase deficiency Is a Enzymopathy true Inferred relationship Existential restriction modifier
Ferrochelatase deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier
Ferrochelatase deficiency Finding site Body system structure false Inferred relationship Existential restriction modifier
Ferrochelatase deficiency Is a Disorder of porphyrin metabolism true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Erythropoietic protoporphyria Is a True Ferrochelatase deficiency Inferred relationship Existential restriction modifier
Erythropoietic protoporphyria due to ferrochelatase deficiency Due to True Ferrochelatase deficiency Inferred relationship Existential restriction modifier 1

This concept is not in any reference sets

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