FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.1  |  FHIR Version n/a  User: [n/a]

367417005: Propionyl-CoA carboxylase deficiency (disorder)

    Status: retired, Primitive. Date: 31-Jul 2002. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    2671104014 Propionyl-CoA carboxylase deficiency [dup] en Synonym Inactive Initial character case insensitive SNOMED CT core
    2741499010 Propionyl-CoA carboxylase deficiency (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
    2769729011 Propionyl-CoA carboxylase deficiency en Synonym Active Initial character case insensitive SNOMED CT core
    491927011 Propionic acidaemia, type I en Synonym Active Initial character case insensitive SNOMED CT core
    491928018 Propionic acidaemia, type II en Synonym Active Initial character case insensitive SNOMED CT core
    491929014 Hyperglycinaemia with ketosis and leucopenia, types I and II en Synonym Active Initial character case insensitive SNOMED CT core
    491930016 Ketotic glycinaemia, types I and II en Synonym Active Initial character case insensitive SNOMED CT core
    491931017 Propionic acidemia, type I en Synonym Active Initial character case insensitive SNOMED CT core
    491932012 Hyperglycinemia with ketosis and leukopenia, types I and II en Synonym Active Initial character case insensitive SNOMED CT core
    491933019 Ketotic glycinemia, types I and II en Synonym Active Initial character case insensitive SNOMED CT core
    491934013 Propionic acidemia, type II en Synonym Active Initial character case insensitive SNOMED CT core
    491935014 Propionyl-CoA carboxylase deficiency (disorder) en Synonym Inactive Initial character case insensitive SNOMED CT core
    775490017 Propionyl-CoA carboxylase deficiency [dup] (disorder) en Fully specified name Inactive Initial character case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Propionyl-CoA carboxylase deficiency Is a Hereditary disorder of haematologic system false Inferred relationship Some
    Propionyl-CoA carboxylase deficiency Is a Leucopenia false Inferred relationship Some
    Propionyl-CoA carboxylase deficiency Is a Hyperglycinaemia false Inferred relationship Some
    Propionyl-CoA carboxylase deficiency Is a Propionic acidaemia false Inferred relationship Some
    Propionyl-CoA carboxylase deficiency Is a Congenital anomaly of the haematopoietic system false Inferred relationship Some
    Propionyl-CoA carboxylase deficiency Is a Autosomal recessive hereditary disorder false Inferred relationship Some
    Propionyl-CoA carboxylase deficiency Is a Enzymopathy false Inferred relationship Some
    Propionyl-CoA carboxylase deficiency Finding site Leucocyte false Inferred relationship Some
    Propionyl-CoA carboxylase deficiency Finding site Haematopoietic system structure false Inferred relationship Some
    Propionyl-CoA carboxylase deficiency Occurrence Congenital false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Propionyl-CoA carboxylase deficiency pccA complementation group Is a False Propionyl-CoA carboxylase deficiency Inferred relationship Some
    Propionyl-CoA carboxylase deficiency pccBC complementation group Is a False Propionyl-CoA carboxylase deficiency Inferred relationship Some

    Reference Sets

    Australian dialect reference set

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

    Back to Start