FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

636691000000104: Congenital pigmentary skin anomaly NOS (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 01-Oct 2012. Module: SNOMED CT United Kingdom clinical extension module

    Descriptions:

    Id Description Lang Type Status Case? Module
    1402821000000111 Congenital pigmentary skin anomaly NOS en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module
    1402831000000113 Congenital pigmentary skin anomaly NOS (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital pigmentary skin anomaly NOS Is a Congenital pigmentary skin anomalies false Inferred relationship Existential restriction modifier
    Congenital pigmentary skin anomaly NOS Occurrence Congenital false Inferred relationship Existential restriction modifier
    Congenital pigmentary skin anomaly NOS Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Congenital pigmentary skin anomaly NOS Associated morphology Pigment alteration false Inferred relationship Existential restriction modifier 2
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Existential restriction modifier 2

    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

    Back to Start