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55056006: Hepatic porphyria (disorder)


Status: current, 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
441851000241117 porphyrie hépatique (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
50007981000188119 porphyrie hépatique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
793355018 Hepatic porphyria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
91537011 Hepatic porphyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


10 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
porphyrie hépatique (trouble) est un(e) (attribut) Disorder of porphyrin metabolism false Inferred relationship Some
porphyrie hépatique (trouble) est un(e) (attribut) Congenital anomaly of trunk false Inferred relationship Some
porphyrie hépatique (trouble) est un(e) (attribut) Digestive system hereditary disorder false Inferred relationship Some
porphyrie hépatique (trouble) est un(e) (attribut) affection du foie true Inferred relationship Some
porphyrie hépatique (trouble) est un(e) (attribut) Congenital anomaly of digestive system false Inferred relationship Some
porphyrie hépatique (trouble) est un(e) (attribut) Porphyria false Inferred relationship Some
porphyrie hépatique (trouble) est un(e) (attribut) Porphyria (disorder) true Inferred relationship Some
porphyrie hépatique (trouble) localisation d'une constatation (attribut) foie true Inferred relationship Some 1
porphyrie hépatique (trouble) survenue (attribut) congénital false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
cholestase intrahépatique récurrente bénigne (trouble) est un(e) (attribut) False porphyrie hépatique (trouble) Inferred relationship Some
syndrome de Rotor (trouble) est un(e) (attribut) False porphyrie hépatique (trouble) Inferred relationship Some
syndrome de Dubin-Johnson est un(e) (attribut) False porphyrie hépatique (trouble) Inferred relationship Some
Familial arthrogryposis-cholestatic hepatorenal syndrome est un(e) (attribut) False porphyrie hépatique (trouble) Inferred relationship Some
Progressive intrahepatic cholestasis est un(e) (attribut) False porphyrie hépatique (trouble) Inferred relationship Some
Crigler-Najjar syndrome, type I est un(e) (attribut) False porphyrie hépatique (trouble) Inferred relationship Some
porphyrie variegata (trouble) est un(e) (attribut) True porphyrie hépatique (trouble) Inferred relationship Some
Porphyria cutanea tarda est un(e) (attribut) True porphyrie hépatique (trouble) Inferred relationship Some
Hereditary coproporphyria est un(e) (attribut) True porphyrie hépatique (trouble) Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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