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69080001: Propionic acidemia (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
114737015 Propionic acidemia en Synonym Active Entire term case insensitive SNOMED CT core module
501182014 Propionic acidaemia en Synonym Active Entire term case insensitive SNOMED CT core module
501184010 Ketotic glycinaemia en Synonym Active Entire term case insensitive SNOMED CT core module
501185011 Ketotic hyperglycinaemia en Synonym Active Entire term case insensitive SNOMED CT core module
501186012 Hyperglycinaemia with ketosis and leucopenia en Synonym Active Entire term case insensitive SNOMED CT core module
501187015 Hyperglycinemia with ketosis and leukopenia en Synonym Active Entire term case insensitive SNOMED CT core module
501188013 Ketotic glycinemia en Synonym Active Entire term case insensitive SNOMED CT core module
501189017 Ketotic hyperglycinemia en Synonym Active Entire term case insensitive SNOMED CT core module
808985015 Propionic acidemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1788119013 Propionyl-CoA carboxylase deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
1788120019 PCC - Propionyl-CoA carboxylase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
4553891013 Propionic aciduria en Synonym Active Entire term case insensitive SNOMED CT core module

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Propionic acidemia Is a Acidemia true Inferred relationship Existential restriction modifier
Propionic acidemia Is a Disorder of propionate AND/OR methylmalonate metabolism true Inferred relationship Existential restriction modifier
Propionic acidemia Is a Non-amino organic acidemia AND/OR aciduria true Inferred relationship Existential restriction modifier
Propionic acidemia Finding site Body system structure false Inferred relationship Existential restriction modifier
Propionic acidemia Is a Disorder of branched-chain amino acid metabolism true Inferred relationship Existential restriction modifier
Propionic acidemia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Propionic acidemia Is a Enzymopathy true Inferred relationship Existential restriction modifier
Propionic acidemia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Propionic acidemia Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Biotin-(propionyl-coenzyme A-carboxylase) ligase deficiency Is a False Propionic acidemia Inferred relationship Existential restriction modifier
Propionyl-CoA carboxylase deficiency Is a False Propionic acidemia Inferred relationship Existential restriction modifier
Propionyl-coenzyme A carboxylase deficiency pccA complementation group Is a True Propionic acidemia Inferred relationship Existential restriction modifier
Propionyl-coenzyme A carboxylase deficiency pccBC complementation group Is a True Propionic acidemia Inferred relationship Existential restriction modifier
Propionic acidemia, type I Is a True Propionic acidemia Inferred relationship Existential restriction modifier
Propionic acidemia, type II Is a True Propionic acidemia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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