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

389197004: Microcephalic osteodysplastic dysplasia (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    1463376015 Microcephalic osteodysplastic dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1483249013 Microcephalic osteodysplastic dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    311151000077114 dysplasie ostéodysplasique microcéphalique type Saul-Wilson fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Associated morphology Congenital dysplasia false Inferred relationship Some 1
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Is a microcéphalie false Inferred relationship Some
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Is a Osteoplastic dysplasia (disorder) false Inferred relationship Some
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Is a Congenital anomaly of head false Inferred relationship Some
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Occurrence Congenital false Inferred relationship Some
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Finding site Brain structure false Inferred relationship Some
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Finding site Bone structure false Inferred relationship Some 1
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Associated morphology Congenital dysplasia false Inferred relationship Some 1
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Finding site Bone structure false Inferred relationship Some 1
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Associated morphology Congenital smallness false Inferred relationship Some 2
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Is a Congenital anomaly of brain false Inferred relationship Some
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Finding site Entire brain false Inferred relationship Some 2
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Occurrence Congenital false Inferred relationship Some 3
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Finding site Bone structure false Inferred relationship Some 3
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Associated morphology Congenital dysplasia false Inferred relationship Some 3
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Associated morphology Congenital smallness false Inferred relationship Some 1
    dysplasie ostéodysplasique microcéphalique type Saul-Wilson Finding site Brain structure false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

    Back to Start