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

77807009: Complete trisomy 10 syndrome (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    129130012 Complete trisomy 10 syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
    818678012 Complete trisomy 10 syndrome (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
    Complete trisomy 10 syndrome Is a Anomaly of chromosome pair 10 false Inferred relationship Existential restriction modifier
    Complete trisomy 10 syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
    Complete trisomy 10 syndrome Finding site Sex chromosome false Inferred relationship Existential restriction modifier
    Complete trisomy 10 syndrome Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
    Complete trisomy 10 syndrome Finding site Chromosome pair 10 false Inferred relationship Existential restriction modifier 1
    Complete trisomy 10 syndrome Associated morphology Trisomy false Inferred relationship Existential restriction modifier 2
    Complete trisomy 10 syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Complete trisomy 10 syndrome Finding site Chromosome pair 10 false Inferred relationship Existential restriction modifier 1
    Complete trisomy 10 syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
    Complete trisomy 10 syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Complete trisomy 10 syndrome Finding site Chromosome pair 10 false Inferred relationship Existential restriction modifier 1
    Complete trisomy 10 syndrome Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

    Back to Start