Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Propionyl-CoA carboxylase deficiency | est un(e) (attribut) | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
Propionyl-CoA carboxylase deficiency | est un(e) (attribut) | Enzymopathy | false | Inferred relationship | Some | ||
Propionyl-CoA carboxylase deficiency | est un(e) (attribut) | Disorder of branched-chain amino acid metabolism | false | Inferred relationship | Some | ||
Propionyl-CoA carboxylase deficiency | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
Propionyl-CoA carboxylase deficiency | survenue (attribut) | congénital | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Propionyl-coenzyme A carboxylase deficiency pccA complementation group (disorder) | est un(e) (attribut) | False | Propionyl-CoA carboxylase deficiency | Inferred relationship | Some | |
Propionyl-coenzyme A carboxylase deficiency pccBC complementation group (disorder) | est un(e) (attribut) | False | Propionyl-CoA carboxylase deficiency | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)