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

88327006: Noonan syndrome (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2004. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    146437010 Noonan syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
    146438017 Turner-like syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
    146439013 Noonan-Ehmke syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
    146440010 Ullrich-Turner syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
    830987011 Noonan syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Noonan syndrome Is a Multiple malformation syndrome, moderate short stature, facial false Inferred relationship Existential restriction modifier
    Noonan syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
    Noonan syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier

    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

    Back to Start