Version 2.77

Description

Porphyrins are created as byproducts of porphyrinogens. Hereditary enzyme disorders leading to the buildup of porphyrins or porphyrinogens cause porphyrias and affect the heme biosynthetic pathway. Most of these disorders are inherited as autosomal dominant disorders. Increased urine porphyrins are seen with congenital erythropoietic porphyria, acute intermittent porphyria, hereditary coproporphyria, variegate porphyria, and porphyria cutanea tarda. Information from LOINC partner 1 and Jacobs and DeMott Laboratory Test Handbook, 5th edition, DS Jacobs, WR DeMott and DK Oxley, 2001. Source: Regenstrief Institute

Basic Part Properties

Part Display Name
Heptacarboxylporphyrin I
Part Type
Component (Describes the core component or analyte measured)
Created On
2000-05-04
Construct for LOINC Short Name
Hepta-CP I

LOINC Terminology Service (API) using HL7® FHIR® Get Info

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=LP14335-1
ConceptMap translate
https://fhir.loinc.org/ConceptMap/$translate?system=http://loinc.org&code=LP14335-1

Language Variants Get Info

Tag Language Translation
zh-CN Chinese (China) 七羧基卟啉 I
Synonyms: Heptacarbox;Hepta-CP I;Hepta-CP1;七羧基卟啉Ⅰ
fr-CA French (Canada) Heptacarboxyporphyrine I
et-EE Estonian (Estonia) Heptakarboksüülporfüriin I
es-ES Spanish (Spain) Heptacarboxilporfirina I
it-IT Italian (Italy) Eptacarbossilporfirina I
tr-TR Turkish (Turkey) Heptakarboksilporfirin I
ru-RU Russian (Russian Federation) Гептакарбоксилпорфирин I
nl-NL Dutch (Netherlands) heptacarboxylporfyrine I
fr-BE French (Belgium) Heptacarboxyporphyrine I