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

402783001: Congenital/hereditary cutis laxa (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    1770707019 Congenital/hereditary cutis laxa (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    1781877014 Congenital/hereditary cutis laxa en Synonym Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital/hereditary cutis laxa Is a Cutis laxa false Inferred relationship Existential restriction modifier
    Congenital/hereditary cutis laxa Finding site Connective tissue structure false Inferred relationship Existential restriction modifier
    Congenital/hereditary cutis laxa Finding site Skin structure false Inferred relationship Existential restriction modifier
    Congenital/hereditary cutis laxa Occurrence Congenital false Inferred relationship Existential restriction modifier
    Congenital/hereditary cutis laxa Is a Congenital connective tissue disorder false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Cutis laxa secondary to inherited disorder of connective tissue Is a False Congenital/hereditary cutis laxa Inferred relationship Existential restriction modifier
    Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome Is a False Congenital/hereditary cutis laxa Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

    Back to Start