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723361006: Familial multiple fibrofolliculoma (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
    3424234017 Familial multiple fibrofolliculoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3424235016 Familial multiple fibrofolliculoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3424236015 A genodermatosis with characteristics of the presence of multiple hamartomas of the hair follicle. It has been described in one family so far. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3424234017 Familial multiple fibrofolliculoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3424235016 Familial multiple fibrofolliculoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3424236015 A genodermatosis with characteristics of the presence of multiple hamartomas of the hair follicle. It has been described in one family so far. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    875231000172114 fibrofolliculomes multiples familiaux fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    875231000172114 fibrofolliculomes multiples familiaux 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
    fibrofolliculomes multiples familiaux Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    fibrofolliculomes multiples familiaux Is a Familial neoplastic disease false Inferred relationship Existential restriction modifier (core metadata concept)
    fibrofolliculomes multiples familiaux Is a Genodermatosis false Inferred relationship Existential restriction modifier (core metadata concept)
    fibrofolliculomes multiples familiaux Is a Fibrofolliculoma false Inferred relationship Existential restriction modifier (core metadata concept)
    fibrofolliculomes multiples familiaux Is a Hereditary disorder of the integument (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    fibrofolliculomes multiples familiaux Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    fibrofolliculomes multiples familiaux Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
    fibrofolliculomes multiples familiaux Associated morphology Follicular fibroma false Inferred relationship Existential restriction modifier (core metadata concept) 2
    fibrofolliculomes multiples familiaux Finding site Hair follicle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    fibrofolliculomes multiples familiaux Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
    fibrofolliculomes multiples familiaux Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    fibrofolliculomes multiples familiaux Associated morphology Follicular fibroma false Inferred relationship Existential restriction modifier (core metadata concept) 1
    fibrofolliculomes multiples familiaux Finding site Hair follicle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    fibrofolliculomes multiples familiaux Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    fibrofolliculomes multiples familiaux Pathological process (attribute) Pathological developmental process (qualifier value) 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)

    REPLACED BY association reference set (foundation metadata concept)

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