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1216941002: Ketoacidosis due to monocarboxylate transporter-1 deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Apr 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5033749012 Ketoacidosis due to monocarboxylate transporter-1 deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5033750012 Ketoacidosis due to monocarboxylate transporter-1 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
Ketoacidosis due to monocarboxylate transporter-1 deficiency Is a Metabolic disorder of transport true Inferred relationship Existential restriction modifier
Ketoacidosis due to monocarboxylate transporter-1 deficiency Is a Autosomal hereditary disorder true Inferred relationship Existential restriction modifier
Ketoacidosis due to monocarboxylate transporter-1 deficiency Is a Ketoacidosis true Inferred relationship Existential restriction modifier
Ketoacidosis due to monocarboxylate transporter-1 deficiency Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier
Ketoacidosis due to monocarboxylate transporter-1 deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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