FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

237953006: Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency - potassium stimulated (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
356637013 Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency - potassium stimulated en Synonym Active Only initial character case insensitive SNOMED CT core module
356638015 Beta-ketothiolase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
626762011 Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency - potassium stimulated (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency - potassium stimulated Is a Deficiency of acetyl-coenzyme A acetyltransferase true Inferred relationship Existential restriction modifier
Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency - potassium stimulated Occurrence Congenital false Inferred relationship Existential restriction modifier
Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency - potassium stimulated Finding site Body system structure false Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start