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111578003: Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2022. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    199731010 Fructose 1,6-biphosphate aldolase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    199732015 Aldolase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1208635014 HNSHA due to aldolase A deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    2618713012 Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to aldolase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2618714018 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to aldolase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2913901014 Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2914382018 Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3780590017 Hereditary nonspherocytic haemolytic anaemia due to aldolase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    178829014 HNSHA due to aldolase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    199731010 Fructose 1,6-biphosphate aldolase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    199732015 Aldolase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    632811014 HNSHA due to aldolase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1185693019 HNSHA due to aldolase A deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1185693019 HNSHA due to aldolase A deficiency (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    1208635014 HNSHA due to aldolase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1208635014 HNSHA due to aldolase A deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    2606396016 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to aldolase A deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2618713012 Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to aldolase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2618714018 Hereditary nonspherocytic hemolytic anemia (HNSHA) due to aldolase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2913901014 Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    2914382018 Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3780590017 Hereditary nonspherocytic haemolytic anaemia due to aldolase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Is a Erythrocyte enzyme deficiency false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Is a Inborn error of metabolism false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Is a Anemia due to enzyme deficiency false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Is a Hereditary disorder of haematologic sysem false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Is a Congenital anomaly of the haematopoietic system false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept) 4
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Is a Hereditary nonspherocytic haemolytic anaemia false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Associated etiologic finding Enzymopathy false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Has definitional manifestation érythropénie false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Due to Enzymopathy false Inferred relationship Existential restriction modifier (core metadata concept) 5
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Has definitional manifestation Hemolysis false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Has interpretation Below reference range false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Has interpretation Below reference range false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Interprets Red blood cell count false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Interprets Measurement of total haemoglobin concentration false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Interprets Erythrocyte destruction false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Has interpretation Present (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Interprets Haemolysis false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    REPLACED BY association reference set (foundation metadata concept)

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