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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. Date: 31-Jan 2022. Module: SNOMED CT core module

    Descriptions:

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

    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
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Is a Inborn error of metabolism false Inferred relationship Existential restriction modifier
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Is a Anemia due to enzyme deficiency false Inferred relationship Existential restriction modifier
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Is a Hereditary disorder of hematologic system false Inferred relationship Existential restriction modifier
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Is a Congenital anomaly of the hematopoietic system false Inferred relationship Existential restriction modifier
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Finding site Erythrocyte false Inferred relationship Existential restriction modifier 4
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Is a Hereditary nonspherocytic hemolytic anemia false Inferred relationship Existential restriction modifier
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Associated etiologic finding Enzymopathy false Inferred relationship Existential restriction modifier
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Has definitional manifestation Erythropenia false Inferred relationship Existential restriction modifier
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Due to Enzymopathy false Inferred relationship Existential restriction modifier 5
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Finding site Body system structure false Inferred relationship Existential restriction modifier
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Has definitional manifestation Hemolysis false Inferred relationship Existential restriction modifier
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Has interpretation Below reference range false Inferred relationship Existential restriction modifier 1
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Has interpretation Below reference range false Inferred relationship Existential restriction modifier 2
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Interprets Red blood cell count false Inferred relationship Existential restriction modifier 1
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Interprets Measurement of total hemoglobin concentration false Inferred relationship Existential restriction modifier 2
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Interprets Erythrocyte destruction, function false Inferred relationship Existential restriction modifier
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Has interpretation Present false Inferred relationship Existential restriction modifier 3
    Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Interprets Hemolysis false Inferred relationship Existential restriction modifier 3
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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