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254135003: Craniometaphyseal dysplasia - mild type (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2026. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    378308014 Craniometaphyseal dysplasia - mild type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    644985010 Craniometaphyseal dysplasia - mild type (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
    Craniometaphyseal dysplasia - mild type Is a Craniometaphyseal dysplasia false Inferred relationship Some
    Craniometaphyseal dysplasia - mild type Associated morphology Dysplasia false Inferred relationship Some 1
    Craniometaphyseal dysplasia - mild type Finding site Bone structure false Inferred relationship Some 1
    Craniometaphyseal dysplasia - mild type Severity Mild false Inferred relationship Some
    Craniometaphyseal dysplasia - mild type Occurrence Congenital false Inferred relationship Some
    Craniometaphyseal dysplasia - mild type Finding site Skeletal system structure false Inferred relationship Some 1
    Craniometaphyseal dysplasia - mild type Finding site Head structure false Inferred relationship Some 2
    Craniometaphyseal dysplasia - mild type Associated morphology Congenital dysplasia false Inferred relationship Some 1
    Craniometaphyseal dysplasia - mild type Associated morphology Congenital malformation false Inferred relationship Some
    Craniometaphyseal dysplasia - mild type Associated morphology Congenital anomaly false Inferred relationship Some 2
    Craniometaphyseal dysplasia - mild type Finding site Bone structure false Inferred relationship Some 1
    Craniometaphyseal dysplasia - mild type Associated morphology Congenital anomaly false Inferred relationship Some 2
    Craniometaphyseal dysplasia - mild type Finding site Head structure false Inferred relationship Some 2
    Craniometaphyseal dysplasia - mild type Associated morphology Congenital dysplasia false Inferred relationship Some 1
    Craniometaphyseal dysplasia - mild type Occurrence Congenital false Inferred relationship Some 3
    Craniometaphyseal dysplasia - mild type Occurrence Congenital false Inferred relationship Some 4
    Craniometaphyseal dysplasia - mild type Associated morphology Developmental anomaly (morphologic abnormality) false Inferred relationship Some 4
    Craniometaphyseal dysplasia - mild type Finding site Head structure false Inferred relationship Some 4
    Craniometaphyseal dysplasia - mild type Associated morphology Dysplasia false Inferred relationship Some 3
    Craniometaphyseal dysplasia - mild type Finding site Bone structure false Inferred relationship Some 3
    Craniometaphyseal dysplasia - mild type Associated morphology Congenital dysplasia false Inferred relationship Some 3
    Craniometaphyseal dysplasia - mild type Occurrence Congenital false Inferred relationship Some 1
    Craniometaphyseal dysplasia - mild type Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 2
    Craniometaphyseal dysplasia - mild type Occurrence Congenital false Inferred relationship Some 2
    Craniometaphyseal dysplasia - mild type Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    Craniometaphyseal dysplasia - mild type Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
    Craniometaphyseal dysplasia - mild type Interprets Bone density scan false Inferred relationship Some 1
    Craniometaphyseal dysplasia - mild type Pathological process (attribute) Pathological developmental process false Inferred relationship Some 3
    Craniometaphyseal dysplasia - mild type Has interpretation Above reference range false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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