FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

37200009: trouble du métabolisme de la tyrosine (trouble)


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
2817041019 Disorder of tyrosine metabolism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
422501000241113 trouble du métabolisme de la tyrosine (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
486652014 Disorder of tyrosine metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
62062013 Disturbance of tyrosine metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
976871000172110 trouble du métabolisme de la tyrosine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


23 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Disorder of tyrosine metabolism (disorder) est un(e) (attribut) Disorder of amino acid metabolism false Inferred relationship Some
Disorder of tyrosine metabolism (disorder) est un(e) (attribut) Disorder of amino acid and organic acid metabolism true Inferred relationship Some
Disorder of tyrosine metabolism (disorder) localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Disorder of tyrosine metabolism (disorder) survenue (attribut) congénital false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Tyrosinase-negative oculocutaneous albinism est un(e) (attribut) True Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Tyrosinuria est un(e) (attribut) True Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Homogentisate 1,2-dioxygenase deficiency est un(e) (attribut) True Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Hepatic tyrosine aminotransferase deficiency est un(e) (attribut) True Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Albinism est un(e) (attribut) False Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Alcaptonuria est un(e) (attribut) False Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Hypertyrosinaemia est un(e) (attribut) True Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Tyrosinosis (disorder) est un(e) (attribut) True Disorder of tyrosine metabolism (disorder) Inferred relationship Some
4-Hydroxyphenylpyruvate dioxygenase deficiency (disorder) est un(e) (attribut) True Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Hypopigmentation-immunodeficiency disease est un(e) (attribut) True Disorder of tyrosine metabolism (disorder) Inferred relationship Some
albinoïdisme est un(e) (attribut) False Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Woolf's syndrome est un(e) (attribut) True Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Brown oculocutaneous albinism Due to False Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Cross syndrome Due to False Disorder of tyrosine metabolism (disorder) Inferred relationship Some
albinisme oculo-cutané type 2 (trouble) Due to False Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Rufous albinism Due to False Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Hermansky-Pudlak syndrome Due to False Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Tyrosinemia est un(e) (attribut) True Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Homogentisic acid defect est un(e) (attribut) False Disorder of tyrosine metabolism (disorder) Inferred relationship Some
Disorder of catecholamine synthesis est un(e) (attribut) True Disorder of tyrosine metabolism (disorder) Inferred relationship Some

This concept is not in any reference sets

Back to Start