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84193000: Trehalase 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
139627012 Trehalose intolerance en Synonym Active Entire term case insensitive SNOMED CT core module
201127011 Trehalase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
1234911010 Alpha, alpha-trehalase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
4636710019 Trehalase 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
Trehalase deficiency Is a Disorder of carbohydrate transport true Inferred relationship Existential restriction modifier
Trehalase deficiency Is a Enzymopathy false Inferred relationship Existential restriction modifier
Trehalase deficiency Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
Trehalase deficiency Is a Disorder of carbohydrate absorption true Inferred relationship Existential restriction modifier
Trehalase deficiency Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier
Trehalase deficiency Finding site Body system structure false Inferred relationship Existential restriction modifier
Trehalase deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Trehalase deficiency Is a Specific enzyme deficiency true Inferred relationship Existential restriction modifier
Trehalase deficiency Is a Autosomal hereditary disorder 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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