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254126005: Osteomesopycnosis (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    378293011 Osteomesopycnosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    644975014 Osteomesopycnosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1454871000005119 Osteomesopyknose da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Osteomesopyknose Is a A very rare benign bone disorder with characteristics of bone dysplasia manifested by patchy sclerosis of the axial skeleton and increased bone mineral content. The disease may be underdiagnosed due to confusion with autosomal dominant osteopetrosis. The condition is usually found incidentally on radiological examination and is very mild, sometimes accompanied by pain. Increased density of the vertebral plates, pelvis and occasionally of the upper femur have been reported, as well as kyphoscoliosis and femoral cysts. false Inferred relationship Some
    Osteomesopyknose Associated morphology Bony sclerosis false Inferred relationship Some
    Osteomesopyknose Associated morphology Dysplasia false Inferred relationship Some 1
    Osteomesopyknose Finding site Bone structure of spine false Inferred relationship Some 1
    Osteomesopyknose Finding site Skeletal system structure false Inferred relationship Some 1
    Osteomesopyknose Occurrence Congenital false Inferred relationship Some
    Osteomesopyknose Associated morphology kongenit dysplasi false Inferred relationship Some 1
    Osteomesopyknose Finding site Bone structure of spine false Inferred relationship Some 1
    Osteomesopyknose Associated morphology kongenit dysplasi false Inferred relationship Some 1
    Osteomesopyknose Occurrence Congenital false Inferred relationship Some 2
    Osteomesopyknose Finding site Bone structure false Inferred relationship Some 2
    Osteomesopyknose Associated morphology kongenit dysplasi false Inferred relationship Some 2
    Osteomesopyknose Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
    Osteomesopyknose Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    Osteomesopyknose Is a Congenital anomaly of spine false Inferred relationship Some
    Osteomesopyknose Occurrence Congenital false Inferred relationship Some 1
    Osteomesopyknose Pathological process (attribute) Pathological developmental process false Inferred relationship Some 3
    Osteomesopyknose Occurrence Congenital false Inferred relationship Some 3
    Osteomesopyknose Associated morphology Bony sclerosis false Inferred relationship Some 3
    Osteomesopyknose Finding site Bone structure false Inferred relationship Some 3
    Osteomesopyknose Has interpretation Above reference range (qualifier value) false Inferred relationship Some 4
    Osteomesopyknose Interprets Bone density scan false Inferred relationship Some 4
    Osteomesopyknose Clinical course Progressive false Inferred relationship Some 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

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