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

3508009: Osteogenesis imperfecta with blue sclerae (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2003. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    6910013 Osteogenesis imperfecta with blue sclerae en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    6911012 Fragilitas ossium hereditaria tarda en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    6912017 OI type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    6913010 Fragilitas ossium-blue sclerae-otosclerosis syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    6914016 Ekman syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    6915015 van der Hoeve syndrome with deafness en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    6916019 Ekman-Lobstein syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    6917011 Adair-Dighton syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    6918018 Osteogenesis imperfecta, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    6919014 Blue sclerae syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    6920015 Osteopsathyrosis idiopathica tarda en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    6921016 Spurway-Eddowes syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    6922011 Osteogenesis imperfecta tarda en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    6923018 Osteogenesis imperfecta psathyrotica en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    6924012 Lobstein disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    6925013 Eddowes syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    486058012 Osteogenesis imperfecta type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    766679012 Osteogenesis imperfecta with blue sclerae (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Osteogenesis imperfecta with blue sclerae Is a Osteogenesis imperfecta false Inferred relationship Some
    Osteogenesis imperfecta with blue sclerae Is a Congenital anomaly of head false Inferred relationship Some
    Osteogenesis imperfecta with blue sclerae Is a Scleral discoloration false Inferred relationship Some
    Osteogenesis imperfecta with blue sclerae Finding site Skeletal system structure false Inferred relationship Some 1
    Osteogenesis imperfecta with blue sclerae Associated morphology blå färg false Inferred relationship Some 2
    Osteogenesis imperfecta with blue sclerae Finding site Connective tissue structure false Inferred relationship Some
    Osteogenesis imperfecta with blue sclerae Finding site Scleral structure false Inferred relationship Some 1
    Osteogenesis imperfecta with blue sclerae Finding site Bone structure false Inferred relationship Some
    Osteogenesis imperfecta with blue sclerae Finding site Connective tissue false Inferred relationship Some
    Osteogenesis imperfecta with blue sclerae Occurrence Congenital false Inferred relationship Some
    Osteogenesis imperfecta with blue sclerae Associated morphology Dysplasia false Inferred relationship Some 1
    Osteogenesis imperfecta with blue sclerae Is a Hereditary disorder of the visual system (disorder) false Inferred relationship Some
    Osteogenesis imperfecta with blue sclerae Is a Blue sclera (disorder) false Inferred relationship Some
    Osteogenesis imperfecta with blue sclerae Is a Congenital anomaly of eye false Inferred relationship Some
    Osteogenesis imperfecta with blue sclerae Is a Ear, face and neck congenital anomalies false Inferred relationship Some
    Osteogenesis imperfecta with blue sclerae Has definitional manifestation blå sklera false Inferred relationship Some
    Osteogenesis imperfecta with blue sclerae Associated morphology kongenital dysplasi false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta Is a False Osteogenesis imperfecta with blue sclerae Inferred relationship Some
    Osteogenesis imperfecta with blue sclerae AND normal teeth Is a False Osteogenesis imperfecta with blue sclerae Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

    Back to Start