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37200009: Disorder of tyrosine metabolism (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
62062013 Disturbance of tyrosine metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
486652014 Disorder of tyrosine metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2817041019 Disorder of tyrosine metabolism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
62062013 Disturbance of tyrosine metabolism en Synonym (core metadata concept) Active Only initial character 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
486652014 Disorder of tyrosine metabolism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
486652014 Disorder of tyrosine metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
769039015 Disturbance of tyrosine metabolism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2817041019 Disorder of tyrosine metabolism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2817041019 Disorder of tyrosine metabolism (disorder) en Fully specified name 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 Switzerland NRC maintained Module
976871000172110 trouble du métabolisme de la tyrosine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


24 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Disorder of tyrosine metabolism (disorder) Is a Disorder of amino acid metabolism (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of tyrosine metabolism (disorder) Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of tyrosine metabolism (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of tyrosine metabolism (disorder) Is a Disorder of amino acid and organic acid metabolism true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Disorder of catecholamine synthesis (disorder) Is a True Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Tyrosinuria Is a True Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Homogentisate 1,2-dioxygenase deficiency (disorder) Is a True Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hepatic tyrosine aminotransferase deficiency Is a True Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Albinism Is a False Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Alcaptonuria Is a False Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypertyrosinaemia Is a True Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Tyrosinosis Is a True Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
tyrosinémie Is a False Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Homogentisic acid defect Is a False Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
4-Hydroxyphenylpyruvate dioxygenase deficiency (disorder) Is a True Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation-immunodeficiency disease Is a True Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
albinoïdisme Is a False Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Woolf's syndrome (disorder) Is a True Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Brown oculocutaneous albinism Due to False Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cross syndrome Due to False Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Tyrosinase-positive oculocutaneous albinism Due to False Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Rufous albinism Due to False Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hermansky-Pudlak syndrome Due to False Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Tyrosinase-negative oculocutaneous albinism Is a True Disorder of tyrosine metabolism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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