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178935009: Congenital elliptocytosis (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    276861015 Congenital elliptocytosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    276862010 Congenital ovalocytosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    561898014 Congenital elliptocytosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    276861015 Congenital elliptocytosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    276861015 Congenital elliptocytosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    276862010 Congenital ovalocytosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    276862010 Congenital ovalocytosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    561898014 Congenital elliptocytosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    561898014 Congenital elliptocytosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    76151000077111 elliptocytose congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    76151000077111 elliptocytose congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    elliptocytose congénitale Is a Hereditary disorder of haematologic sysem false Inferred relationship Existential restriction modifier (core metadata concept)
    elliptocytose congénitale Is a Erythrocyte membrane abnormality false Inferred relationship Existential restriction modifier (core metadata concept)
    elliptocytose congénitale Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    elliptocytose congénitale Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept)
    elliptocytose congénitale Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    elliptocytose congénitale Is a Congenital anomaly of the haematopoietic system false Inferred relationship Existential restriction modifier (core metadata concept)
    elliptocytose congénitale Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    elliptocytose congénitale Is a Hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
    elliptocytose congénitale Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)
    elliptocytose congénitale Has definitional manifestation Red blood cell finding (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
    elliptocytose congénitale Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
    elliptocytose congénitale Is a Hereditary red blood cell disorder (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    elliptocytose congénitale Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    elliptocytose congénitale Associated morphology Congenital abnormal shape false Inferred relationship Existential restriction modifier (core metadata concept) 1
    elliptocytose congénitale Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept) 1
    elliptocytose congénitale Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    elliptocytose congénitale Associated morphology Abnormal shape (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

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

    SAME AS association reference set (foundation metadata concept)

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