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2298005: Goltz 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
    4954016 Goltz syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    4955015 Focal dermal hypoplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    4956019 Goltz-Gorlin syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    752449013 Goltz syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3035263018 Goltz-Gorlin (dermal hypoplasia) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3036043010 Goltz Gorlin syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    4954016 Goltz syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    4955015 Focal dermal hypoplasia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    4955015 Focal dermal hypoplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    4956019 Goltz-Gorlin syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    752449013 Goltz syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    752449013 Goltz syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    1223007019 Focal facial dermal dysplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3035263018 Goltz-Gorlin (dermal hypoplasia) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3036043010 Goltz Gorlin syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Goltz syndrome Is a Hamartomatous disease false Inferred relationship Existential restriction modifier (core metadata concept)
    Goltz syndrome Is a Congenital anomaly of face false Inferred relationship Existential restriction modifier (core metadata concept)
    Goltz syndrome Is a Nevi, hamartomas and developmental anomalies false Inferred relationship Existential restriction modifier (core metadata concept)
    Goltz syndrome Is a Disorder of skin AND/OR subcutaneous tissue of head (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Goltz syndrome Is a Congenital anomaly of integument false Inferred relationship Existential restriction modifier (core metadata concept)
    Goltz syndrome Finding site Skin of part of face (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    Goltz syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Goltz syndrome Finding site Dermis structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Goltz syndrome Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Goltz syndrome Is a Congenital anomaly of skin (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Goltz syndrome Is a Skin lesion false Inferred relationship Existential restriction modifier (core metadata concept)
    Goltz syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Goltz syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept)
    Goltz syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Goltz syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Goltz syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Goltz syndrome Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Goltz syndrome Finding site Dermis structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Goltz syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Goltz syndrome Is a Congenital hamartoma (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Goltz syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
    Goltz syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept) 4
    Goltz syndrome Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Goltz syndrome Finding site Dermis structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Goltz syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Goltz syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Goltz syndrome Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Goltz syndrome Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Goltz syndrome Occurrence Congenital 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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