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

3508009: Osteogenesis imperfecta with blue sclerae (disorder)


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

    Descriptions:

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


    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 Existential restriction modifier
    Osteogenesis imperfecta with blue sclerae Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier
    Osteogenesis imperfecta with blue sclerae Is a Scleral discoloration false Inferred relationship Existential restriction modifier
    Osteogenesis imperfecta with blue sclerae Finding site Skeletal system structure false Inferred relationship Existential restriction modifier 1
    Osteogenesis imperfecta with blue sclerae Associated morphology Blue color false Inferred relationship Existential restriction modifier 2
    Osteogenesis imperfecta with blue sclerae Finding site Connective tissue structure false Inferred relationship Existential restriction modifier
    Osteogenesis imperfecta with blue sclerae Finding site Scleral structure false Inferred relationship Existential restriction modifier 1
    Osteogenesis imperfecta with blue sclerae Finding site Bone structure false Inferred relationship Existential restriction modifier
    Osteogenesis imperfecta with blue sclerae Finding site Connective tissue false Inferred relationship Existential restriction modifier
    Osteogenesis imperfecta with blue sclerae Occurrence Congenital false Inferred relationship Existential restriction modifier
    Osteogenesis imperfecta with blue sclerae Associated morphology Dysplasia false Inferred relationship Existential restriction modifier 1
    Osteogenesis imperfecta with blue sclerae Is a Hereditary disorder of the visual system false Inferred relationship Existential restriction modifier
    Osteogenesis imperfecta with blue sclerae Is a Blue sclera false Inferred relationship Existential restriction modifier
    Osteogenesis imperfecta with blue sclerae Is a Congenital anomaly of eye false Inferred relationship Existential restriction modifier
    Osteogenesis imperfecta with blue sclerae Is a Ear, face and neck congenital anomalies false Inferred relationship Existential restriction modifier
    Osteogenesis imperfecta with blue sclerae Has definitional manifestation Blue sclerae false Inferred relationship Existential restriction modifier
    Osteogenesis imperfecta with blue sclerae Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 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 Existential restriction modifier
    Osteogenesis imperfecta with blue sclerae AND normal teeth Is a False Osteogenesis imperfecta with blue sclerae Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

    Back to Start