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238014002: Dihydropyrimidinase deficiency (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
356748010 Dihydrouracil amidohydrolase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
356749019 Dihydropyrimidinase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
626832010 Dihydropyrimidinase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dihydropyrimidinase deficiency Is a Disorder of purine and pyrimidine metabolism false Inferred relationship Existential restriction modifier
Dihydropyrimidinase deficiency Is a Disorder of pyrimidine metabolism true Inferred relationship Existential restriction modifier
Dihydropyrimidinase deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier
Dihydropyrimidinase deficiency Finding site Body system structure false Inferred relationship Existential restriction modifier
Dihydropyrimidinase deficiency Is a Enzymopathy true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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