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403778001: X-linked dominant chondrodysplasia punctata of Happle (disorder)

    Status: retired, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    1771704018 X-linked dominant chondrodysplasia punctata of Happle (disorder) en Fully specified name Active Case sensitive SNOMED CT core
    1782788014 X-linked dominant chondrodysplasia punctata of Happle en Synonym Active Case sensitive SNOMED CT core
    1787869018 X-linked dominant ichthyosis (Happle) en Synonym Active Case sensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    X-linked dominant chondrodysplasia punctata of Happle Occurrence Congenital false Inferred relationship Some 1
    X-linked dominant chondrodysplasia punctata of Happle Pathological process Pathological developmental process false Inferred relationship Some 1
    X-linked dominant chondrodysplasia punctata of Happle Associated morphology Dysplasia false Inferred relationship Some 1
    X-linked dominant chondrodysplasia punctata of Happle Is a Hereditary disorder of musculoskeletal system false Inferred relationship Some
    X-linked dominant chondrodysplasia punctata of Happle Is a X-linked hereditary disease false Inferred relationship Some
    X-linked dominant chondrodysplasia punctata of Happle Is a Developmental hereditary disorder false Inferred relationship Some
    X-linked dominant chondrodysplasia punctata of Happle Is a Degenerative disorder of musculoskeletal system false Inferred relationship Some
    X-linked dominant chondrodysplasia punctata of Happle Is a Atrophoderma false Inferred relationship Some
    X-linked dominant chondrodysplasia punctata of Happle Is a Congenital anomaly of skin false Inferred relationship Some
    X-linked dominant chondrodysplasia punctata of Happle Is a Chondrodysplasia punctata false Inferred relationship Some
    X-linked dominant chondrodysplasia punctata of Happle Associated morphology Congenital dysplasia false Inferred relationship Some 1
    X-linked dominant chondrodysplasia punctata of Happle Associated morphology Atrophy false Inferred relationship Some 2
    X-linked dominant chondrodysplasia punctata of Happle Finding site Skin structure false Inferred relationship Some 2
    X-linked dominant chondrodysplasia punctata of Happle Finding site Bone structure false Inferred relationship Some 1
    X-linked dominant chondrodysplasia punctata of Happle Occurrence Congenital false Inferred relationship Some
    X-linked dominant chondrodysplasia punctata of Happle Associated morphology Congenital dysplasia false Inferred relationship Some 1
    X-linked dominant chondrodysplasia punctata of Happle Finding site Bone structure false Inferred relationship Some 1
    X-linked dominant chondrodysplasia punctata of Happle Finding site Skin structure false Inferred relationship Some 2
    X-linked dominant chondrodysplasia punctata of Happle Associated morphology Atrophy false Inferred relationship Some 2
    X-linked dominant chondrodysplasia punctata of Happle Occurrence Congenital false Inferred relationship Some 3
    X-linked dominant chondrodysplasia punctata of Happle Finding site Bone structure false Inferred relationship Some 3
    X-linked dominant chondrodysplasia punctata of Happle Associated morphology Congenital dysplasia false Inferred relationship Some 3
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set

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