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208008: Neurocutaneous melanosis sequence (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    1441015 Neurocutaneous melanosis sequence en Synonym Active Entire term case insensitive SNOMED CT core module
    750024014 Neurocutaneous melanosis sequence (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Neurocutaneous melanosis sequence Is a Miscellaneous disorders of skin pigmentation false Inferred relationship Existential restriction modifier
    Neurocutaneous melanosis sequence Is a Congenital hamartosis false Inferred relationship Existential restriction modifier
    Neurocutaneous melanosis sequence Is a Congenital anomaly of integument false Inferred relationship Existential restriction modifier
    Neurocutaneous melanosis sequence Finding site Structure of skin region false Inferred relationship Existential restriction modifier
    Neurocutaneous melanosis sequence Occurrence Congenital false Inferred relationship Existential restriction modifier
    Neurocutaneous melanosis sequence Associated morphology Melanosis false Inferred relationship Existential restriction modifier 1
    Neurocutaneous melanosis sequence Is a Disorder of skin pigmentation false Inferred relationship Existential restriction modifier
    Neurocutaneous melanosis sequence Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Neurocutaneous melanosis sequence Associated morphology Hamartoma false Inferred relationship Existential restriction modifier
    Neurocutaneous melanosis sequence Is a Melanosis false Inferred relationship Existential restriction modifier
    Neurocutaneous melanosis sequence Associated morphology Melanosis false Inferred relationship Existential restriction modifier 1
    Neurocutaneous melanosis sequence Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Neurocutaneous melanosis sequence Is a Congenital hamartoma false Inferred relationship Existential restriction modifier
    Neurocutaneous melanosis sequence Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Neurocutaneous melanosis sequence Associated morphology Hamartoma false Inferred relationship Existential restriction modifier 2
    Neurocutaneous melanosis sequence Is a Congenital pigmentary skin anomalies false Inferred relationship Existential restriction modifier
    Neurocutaneous melanosis sequence Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Neurocutaneous melanosis sequence Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Neurocutaneous melanosis sequence Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
    Neurocutaneous melanosis sequence Is a Congenital melanosis false Inferred relationship Existential restriction modifier
    Neurocutaneous melanosis sequence Is a Dysplastic nevus of skin false Inferred relationship Existential restriction modifier
    Neurocutaneous melanosis sequence Associated morphology Dysplastic nevus false Inferred relationship Existential restriction modifier 1
    Neurocutaneous melanosis sequence Is a Congenital pigmented melanocytic nevus of skin false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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