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178935009: Congenital elliptocytosis (disorder)

    Status: retired, Primitive. Date: 31-Jan 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    276861015 Congenital elliptocytosis en Synonym Active Case insensitive SNOMED CT core
    276862010 Congenital ovalocytosis en Synonym Active Case insensitive SNOMED CT core
    561898014 Congenital elliptocytosis (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
    Congenital elliptocytosis Pathological process Pathological developmental process false Inferred relationship Some 1
    Congenital elliptocytosis Associated morphology Abnormal shape false Inferred relationship Some 1
    Congenital elliptocytosis Is a Hereditary disorder of haematologic system false Inferred relationship Some
    Congenital elliptocytosis Is a Erythrocyte membrane abnormality false Inferred relationship Some
    Congenital elliptocytosis Finding site Haematopoietic system structure false Inferred relationship Some
    Congenital elliptocytosis Is a Congenital anomaly of the haematopoietic system false Inferred relationship Some
    Congenital elliptocytosis Occurrence Congenital false Inferred relationship Some
    Congenital elliptocytosis Is a Hereditary disease false Inferred relationship Some
    Congenital elliptocytosis Is a Congenital disease false Inferred relationship Some
    Congenital elliptocytosis Has definitional manifestation Red blood cell finding false Inferred relationship Some
    Congenital elliptocytosis Finding site Haematopoietic system structure false Inferred relationship Some
    Congenital elliptocytosis Finding site Erythrocyte false Inferred relationship Some
    Congenital elliptocytosis Is a Congenital anomaly false Inferred relationship Some
    Congenital elliptocytosis Is a Hereditary red blood cell disorder false Inferred relationship Some
    Congenital elliptocytosis Occurrence Congenital false Inferred relationship Some 1
    Congenital elliptocytosis Associated morphology Congenital abnormal shape false Inferred relationship Some 1
    Congenital elliptocytosis Finding site Erythrocyte false Inferred relationship Some 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set

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