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860859009: Erythropoietic protoporphyria due to ferrochelatase deficiency (disorder)


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
3944367018 Erythropoietic protoporphyria due to ferrochelatase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3944368011 Erythropoietic protoporphyria due to ferrochelatase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Erythropoietic protoporphyria due to ferrochelatase deficiency Is a Erythropoietic protoporphyria true Inferred relationship Existential restriction modifier
Erythropoietic protoporphyria due to ferrochelatase deficiency Due to Ferrochelatase deficiency true Inferred relationship Existential restriction modifier 1
Erythropoietic protoporphyria due to ferrochelatase deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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