FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

88327006: Noonan syndrome (disorder)


    Status: retired, Primitive. Date: 31-Jul 2004. Module: SNOMED CT core

    Descriptions:

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


    0 descendants.

    Expanded Value Set


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

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Australian dialect reference set

    Concept inactivation indicator reference set

    SAME AS association reference set

    Back to Start