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1197360001: X-linked dominant erythropoietic protoporphyria (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4696003018 X-linked dominant erythropoietic protoporphyria en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4696006014 X-linked dominant erythropoietic protoporphyria (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
4696004012 A rare disorder of porphyrin and haem metabolism characterised by infantile or childhood onset of severe cutaneous photosensitivity in affected males, presenting as tingling, burning, and itching within minutes of light exposure, often accompanied by swelling and redness of the skin. Pain may persist for hours or days after the initial reaction. Some patients show hepatic involvement and gallstone formation. Laboratory examination reveals increased levels of zinc and metal-free protoporphyrin. The phenotype in heterozygous females ranges from asymptomatic to severe. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4696005013 A rare disorder of porphyrin and heme metabolism characterized by infantile or childhood onset of severe cutaneous photosensitivity in affected males, presenting as tingling, burning, and itching within minutes of light exposure, often accompanied by swelling and redness of the skin. Pain may persist for hours or days after the initial reaction. Some patients show hepatic involvement and gallstone formation. Laboratory examination reveals increased levels of zinc and metal-free protoporphyrin. The phenotype in heterozygous females ranges from asymptomatic to severe. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5630531000052118 X-bunden dominant erytropoetisk protoporfyri sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked dominant erythropoietic protoporphyria Is a X-linked dominant hereditary disease (disorder) true Inferred relationship Some
X-linked dominant erythropoietic protoporphyria Is a Erythropoietic protoporphyria true Inferred relationship Some
X-linked dominant erythropoietic protoporphyria Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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