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2298005: Goltz syndrome (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    4954016 Goltz syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
    4955015 Focal dermal hypoplasia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
    4956019 Goltz-Gorlin syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
    752449013 Goltz syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
    3035263018 Goltz-Gorlin (dermal hypoplasia) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
    3036043010 Goltz Gorlin syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Goltz syndrome Is a Congenital hamartosis false Inferred relationship Existential restriction modifier
    Goltz syndrome Is a Congenital anomaly of face false Inferred relationship Existential restriction modifier
    Goltz syndrome Is a Nevi, hamartomas and developmental anomalies false Inferred relationship Existential restriction modifier
    Goltz syndrome Is a Disorder of skin AND/OR subcutaneous tissue of head false Inferred relationship Existential restriction modifier
    Goltz syndrome Is a Congenital anomaly of integument false Inferred relationship Existential restriction modifier
    Goltz syndrome Finding site Skin of part of face false Inferred relationship Existential restriction modifier
    Goltz syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
    Goltz syndrome Finding site Dermis structure false Inferred relationship Existential restriction modifier 1
    Goltz syndrome Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier 1
    Goltz syndrome Is a Congenital anomaly of skin false Inferred relationship Existential restriction modifier
    Goltz syndrome Is a Skin lesion false Inferred relationship Existential restriction modifier
    Goltz syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
    Goltz syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier
    Goltz syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Goltz syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
    Goltz syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Goltz syndrome Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier 1
    Goltz syndrome Finding site Dermis structure false Inferred relationship Existential restriction modifier 1
    Goltz syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
    Goltz syndrome Is a Congenital hamartoma false Inferred relationship Existential restriction modifier
    Goltz syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
    Goltz syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier 4
    Goltz syndrome Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier 3
    Goltz syndrome Finding site Dermis structure false Inferred relationship Existential restriction modifier 3
    Goltz syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Goltz syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier 2
    Goltz syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
    Goltz syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Goltz syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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