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725103004: Bowed tibia, radial anomaly, osteopenia, fracture syndrome (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
    3438582012 Bowed tibia, radial anomaly, osteopenia, fracture syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    3438583019 Bowed tibia, radial anomaly, osteopenia, fracture syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
    3438584013 Chitty Hall Webb syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Bowed tibia, radial anomaly, osteopenia, fracture syndrome Is a Dysplasia with decreased bone density false Inferred relationship Existential restriction modifier
    Bowed tibia, radial anomaly, osteopenia, fracture syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
    Bowed tibia, radial anomaly, osteopenia, fracture syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Bowed tibia, radial anomaly, osteopenia, fracture syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 2
    Bowed tibia, radial anomaly, osteopenia, fracture syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
    Bowed tibia, radial anomaly, osteopenia, fracture syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Bowed tibia, radial anomaly, osteopenia, fracture syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 1
    Bowed tibia, radial anomaly, osteopenia, fracture syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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