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205490002: Osteodysplasia (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
    315109012 Osteodysplasia en Synonym Active Entire term case insensitive SNOMED CT core module
    590864016 Osteodysplasia (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
    Osteodysplasia Is a Congenital skeletal dysplasia false Inferred relationship Existential restriction modifier
    Osteodysplasia Finding site Bone structure false Inferred relationship Existential restriction modifier 1
    Osteodysplasia Associated morphology Dysplasia false Inferred relationship Existential restriction modifier 1
    Osteodysplasia Finding site Skeletal system structure false Inferred relationship Existential restriction modifier 1
    Osteodysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier
    Osteodysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
    Osteodysplasia Finding site Bone structure false Inferred relationship Existential restriction modifier 1
    Osteodysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
    Osteodysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Osteodysplasia Finding site Bone structure false Inferred relationship Existential restriction modifier 2
    Osteodysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
    Osteodysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Osteodysplasia Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Osteochondrodysplasia Is a False Osteodysplasia Inferred relationship Existential restriction modifier
    Osteodysplasia, unspecified Is a False Osteodysplasia Inferred relationship Existential restriction modifier
    Other osteodysplasia NOS Is a False Osteodysplasia Inferred relationship Existential restriction modifier
    Other specified osteodysplasia Is a False Osteodysplasia Inferred relationship Existential restriction modifier
    Osteodysplasia NOS Is a False Osteodysplasia Inferred relationship Existential restriction modifier
    Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Is a False Osteodysplasia Inferred relationship Existential restriction modifier
    Oto-palato-digital syndrome, type II Is a False Osteodysplasia Inferred relationship Existential restriction modifier
    Oto-palato-digital syndrome, type I Is a False Osteodysplasia Inferred relationship Existential restriction modifier
    Otopalatodigital syndrome Is a False Osteodysplasia Inferred relationship Existential restriction modifier
    Familial osteodysplasia Anderson type Is a False Osteodysplasia Inferred relationship Existential restriction modifier
    Other specified osteodysplasia Is a False Osteodysplasia Inferred relationship Existential restriction modifier
    Osteodysplasia NOS Is a False Osteodysplasia Inferred relationship Existential restriction modifier
    Osteodysplasia, unspecified Is a False Osteodysplasia Inferred relationship Existential restriction modifier
    Other osteodysplasia NOS Is a False Osteodysplasia Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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