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37200009: Disorder of tyrosine metabolism (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
62062013 Disturbance of tyrosine metabolism en Synonym Active Entire term case insensitive SNOMED CT core module
486652014 Disorder of tyrosine metabolism en Synonym Active Entire term case insensitive SNOMED CT core module
2817041019 Disorder of tyrosine metabolism (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

25 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Disorder of tyrosine metabolism Is a Disorder of amino acid metabolism false Inferred relationship Existential restriction modifier
Disorder of tyrosine metabolism Finding site Body system structure false Inferred relationship Existential restriction modifier
Disorder of tyrosine metabolism Occurrence Congenital false Inferred relationship Existential restriction modifier
Disorder of tyrosine metabolism Is a Disorder of amino acid and organic acid metabolism true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Disorder of catecholamine synthesis Is a True Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Tyrosinuria Is a True Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Homogentisate 1,2-dioxygenase deficiency Is a True Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Hepatic tyrosine aminotransferase deficiency Is a True Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Albinism Is a False Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Alcaptonuria Is a False Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Hypertyrosinemia Is a True Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Tyrosinosis Is a True Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Tyrosinemia Is a True Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Homogentisic acid defect Is a False Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
4-Hydroxyphenylpyruvate dioxygenase deficiency Is a True Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Is a True Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Albinoidism Is a False Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Woolf's syndrome Is a True Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Brown oculocutaneous albinism Due to False Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Cross syndrome Due to False Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Tyrosinase-positive oculocutaneous albinism Due to False Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Rufous albinism Due to False Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Hermansky-Pudlak syndrome Due to False Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier
Tyrosinase-negative oculocutaneous albinism Is a True Disorder of tyrosine metabolism Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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