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718558008: Mevalonic aciduria (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3312758018 Mevalonic aciduria (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3312759014 Mevalonic aciduria en Synonym Active Entire term case insensitive SNOMED CT core module
3312760016 Complete mevalonate kinase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mevalonic aciduria Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Mevalonic aciduria Is a Deficiency of mevalonate kinase 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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