FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

238053006: Homozygous erythropoietic protoporphyria (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
356833014 Homozygous erythropoietic protoporphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626882017 Homozygous erythropoietic protoporphyria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
356833014 Homozygous erythropoietic protoporphyria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
356833014 Homozygous erythropoietic protoporphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626882017 Homozygous erythropoietic protoporphyria (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
626882017 Homozygous erythropoietic protoporphyria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5021681000241117 protoporphyrie érythropoiètique homozygote fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5021681000241117 protoporphyrie érythropoiètique homozygote fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Homozygous erythropoietic protoporphyria Is a Erythropoietic protoporphyria true Inferred relationship Existential restriction modifier (core metadata concept)
Homozygous erythropoietic protoporphyria Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Homozygous erythropoietic protoporphyria Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start