56051008: Ketoacidosis (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Metabolic disease\Disorder of acid-base balance\Acidosis\Metabolic acidosis\Metabolic acidosis, increased anion gap (IAG)\Metabolic acidosis, IAG, accumulation of organic acids\Ketoacidosis

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

Descriptions:

Id Description Lang Type Status Case? Module

93235011 Ketoacidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

794521011 Ketoacidosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3422651000005110 ketoacidose da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Ketoacidosis	Is a	Metabolic acidosis, IAG, accumulation of organic acids	true	Inferred relationship	Some
Ketoacidosis	Finding site	Body system structure	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Diabetes med ketoacidose	Is a	False	Ketoacidosis	Inferred relationship	Some
Ketosis	Is a	False	Ketoacidosis	Inferred relationship	Some
Starvation ketoacidosis	Is a	True	Ketoacidosis	Inferred relationship	Some
Ketoacidosis due to acute alcohol intoxication	Is a	True	Ketoacidosis	Inferred relationship	Some
Ketoacidemia NEC	Is a	False	Ketoacidosis	Inferred relationship	Some
Diabetic ketoacidosis	Is a	True	Ketoacidosis	Inferred relationship	Some
A rare disorder of ketone body transport characterised by recurrent episodes of ketoacidosis provoked by fasting or infections in the first years of life. The episodes are typically preceded by poor feeding and vomiting and are associated with dehydration, in severe cases also with decreased consciousness and insufficient respiratory drive. Hypoglycaemia is observed only infrequently. Patients with homozygous mutations tend to present at a younger age, have more profound ketoacidosis, and may show mild to moderate developmental delay in addition.	Is a	True	Ketoacidosis	Inferred relationship	Some

This concept is not in any reference sets