FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.3  |  FHIR Version n/a  User: [n/a]

123768009: Hereditary methemoglobinemia, enzymatic type (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    192257013 Hereditary methemoglobinemia, enzymatic type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    203424018 Hereditary methaemoglobinaemia, enzymatic type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    726848012 Hereditary methemoglobinemia, enzymatic type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1826821000005116 Hereditær methæmoglobinæmi, enzymatisk type da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Hereditær methæmoglobinæmi, enzymatisk type Is a Inborn error of metabolism false Inferred relationship Some
    Hereditær methæmoglobinæmi, enzymatisk type Is a Hereditary disorder of hematologic system false Inferred relationship Some
    Hereditær methæmoglobinæmi, enzymatisk type Is a Autosomal recessive hereditary disorder false Inferred relationship Some
    Hereditær methæmoglobinæmi, enzymatisk type Is a Enzymopathy false Inferred relationship Some
    Hereditær methæmoglobinæmi, enzymatisk type Is a Methemoglobinemia false Inferred relationship Some
    Hereditær methæmoglobinæmi, enzymatisk type Is a Congenital anomaly of the hematopoietic system false Inferred relationship Some
    Hereditær methæmoglobinæmi, enzymatisk type Finding site Erythrocyte false Inferred relationship Some
    Hereditær methæmoglobinæmi, enzymatisk type Occurrence Congenital false Inferred relationship Some
    Hereditær methæmoglobinæmi, enzymatisk type Finding site Haematopoietic system structure false Inferred relationship Some
    Hereditær methæmoglobinæmi, enzymatisk type Finding site Haematopoietic system structure false Inferred relationship Some
    Hereditær methæmoglobinæmi, enzymatisk type Has definitional manifestation Red blood cell finding false Inferred relationship Some
    Hereditær methæmoglobinæmi, enzymatisk type Is a Congenital methemoglobinemia false Inferred relationship Some
    Hereditær methæmoglobinæmi, enzymatisk type Is a Hereditary red blood cell disorder (disorder) false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    cytochrom b>3<-mangel Is a False Hereditær methæmoglobinæmi, enzymatisk type Inferred relationship Some
    HNSHA forårsaget af NADH-methæmoglobinreductasemangel Is a False Hereditær methæmoglobinæmi, enzymatisk type Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    Description inactivation indicator reference set

    GB English

    US English

    REPLACED BY association reference set (foundation metadata concept)

    Back to Start