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45167004: Moynahan's syndrome (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
    75318015 Moynahan's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    75319011 Progressive cardiomyopathic lentiginosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    782376016 Moynahan's syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    2842257014 Moynahan syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    75318015 Moynahan's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    75319011 Progressive cardiomyopathic lentiginosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    75319011 Progressive cardiomyopathic lentiginosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    782376016 Moynahan's syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    782376016 Moynahan's syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    2842257014 Moynahan syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    946461000172115 syndrome de Moynahan fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    980251000172114 syndrome d'alopécie, épilepsie, déficience intellectuelle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    946461000172115 syndrome de Moynahan fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    980251000172114 syndrome d'alopécie, épilepsie, déficience intellectuelle 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
    syndrome de Moynahan Is a Ectodermal dysplasia with hair-tooth-nail-sweating defect false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Moynahan Is a Hamartomatous disease false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Moynahan Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Moynahan Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Moynahan Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Moynahan Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Moynahan Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Moynahan Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Moynahan Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Moynahan Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Moynahan Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome de Moynahan Is a Congenital hamartoma (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Moynahan Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome de Moynahan Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome de Moynahan Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome de Moynahan Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome de Moynahan Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome de Moynahan Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
    syndrome de Moynahan Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 4
    syndrome de Moynahan Finding site Ectoderm structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
    syndrome de Moynahan Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept) 4
    syndrome de Moynahan Finding site Structure of skin and/or mucous membrane (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Moynahan Associated morphology Lentigo false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome de Moynahan Is a Lentiginosis false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome de Moynahan Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome de Moynahan Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 4
    syndrome de Moynahan Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome de Moynahan Finding site Ectoderm structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome de Moynahan Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome de Moynahan Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome de Moynahan Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

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

    POSSIBLY EQUIVALENT TO association reference set

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