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123768009: Hereditary methemoglobinemia, enzymatic type (disorder)

    Status: retired, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    192257013 Hereditary methemoglobinemia, enzymatic type en Synonym Active Case insensitive SNOMED CT core
    203424018 Hereditary methaemoglobinaemia, enzymatic type en Synonym Active Case insensitive SNOMED CT core
    726848012 Hereditary methemoglobinemia, enzymatic type (disorder) en Fully specified name Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Hereditary methaemoglobinaemia, enzymatic type Is a Inborn error of metabolism false Inferred relationship Some
    Hereditary methaemoglobinaemia, enzymatic type Is a Hereditary disorder of haematologic system false Inferred relationship Some
    Hereditary methaemoglobinaemia, enzymatic type Is a Autosomal recessive hereditary disorder false Inferred relationship Some
    Hereditary methaemoglobinaemia, enzymatic type Is a Enzymopathy false Inferred relationship Some
    Hereditary methaemoglobinaemia, enzymatic type Is a Methaemoglobinaemia false Inferred relationship Some
    Hereditary methaemoglobinaemia, enzymatic type Is a Congenital anomaly of the haematopoietic system false Inferred relationship Some
    Hereditary methaemoglobinaemia, enzymatic type Finding site Haematopoietic system structure false Inferred relationship Some
    Hereditary methaemoglobinaemia, enzymatic type Has definitional manifestation Red blood cell finding false Inferred relationship Some
    Hereditary methaemoglobinaemia, enzymatic type Is a Congenital methaemoglobinaemia false Inferred relationship Some
    Hereditary methaemoglobinaemia, enzymatic type Is a Hereditary red blood cell disorder false Inferred relationship Some
    Hereditary methaemoglobinaemia, enzymatic type Finding site Erythrocyte false Inferred relationship Some
    Hereditary methaemoglobinaemia, enzymatic type Occurrence Congenital false Inferred relationship Some
    Hereditary methaemoglobinaemia, enzymatic type Finding site Haematopoietic system structure false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Cytochrome b>3< deficiency Is a False Hereditary methaemoglobinaemia, enzymatic type Inferred relationship Some
    HNSHA due to NADH-methaemoglobin reductase deficiency Is a False Hereditary methaemoglobinaemia, enzymatic type Inferred relationship Some

    Reference Sets

    Australian dialect reference set

    Concept inactivation indicator reference set

    REPLACED BY association reference set

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