FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

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
    1887841000052114 Goltz syndrom sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Goltz syndrom Is a hamartos false Inferred relationship Some
    Goltz syndrom Is a Congenital anomaly of face false Inferred relationship Some
    Goltz syndrom Is a Nevi, hamartomas and developmental anomalies false Inferred relationship Some
    Goltz syndrom Is a Disorder of skin AND/OR subcutaneous tissue of head (disorder) false Inferred relationship Some
    Goltz syndrom Is a Congenital anomaly of integument false Inferred relationship Some
    Goltz syndrom Finding site Skin of part of face false Inferred relationship Some
    Goltz syndrom Occurrence Congenital false Inferred relationship Some
    Goltz syndrom Finding site Dermis structure (body structure) false Inferred relationship Some 1
    Goltz syndrom Associated morphology Hypoplasia false Inferred relationship Some 1
    Goltz syndrom Is a Congenital anomaly of skin false Inferred relationship Some
    Goltz syndrom Is a Skin lesion false Inferred relationship Some
    Goltz syndrom Associated morphology kongenital anomali false Inferred relationship Some 2
    Goltz syndrom Associated morphology Hamartoma false Inferred relationship Some
    Goltz syndrom Finding site Skin structure false Inferred relationship Some 2
    Goltz syndrom Associated morphology kongenital anomali false Inferred relationship Some 2
    Goltz syndrom Finding site Skin structure false Inferred relationship Some 2
    Goltz syndrom Associated morphology Hypoplasia false Inferred relationship Some 1
    Goltz syndrom Finding site Dermis structure (body structure) false Inferred relationship Some 1
    Goltz syndrom Occurrence Congenital false Inferred relationship Some 3
    Goltz syndrom Is a Congenital hamartoma (disorder) false Inferred relationship Some
    Goltz syndrom Occurrence Congenital false Inferred relationship Some 4
    Goltz syndrom Associated morphology Hamartoma false Inferred relationship Some 4
    Goltz syndrom Associated morphology Hypoplasia false Inferred relationship Some 3
    Goltz syndrom Finding site Dermis structure (body structure) false Inferred relationship Some 3
    Goltz syndrom Occurrence Congenital false Inferred relationship Some 2
    Goltz syndrom Associated morphology Hamartoma false Inferred relationship Some 2
    Goltz syndrom Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
    Goltz syndrom Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    Goltz syndrom Occurrence Congenital false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

    Back to Start