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239068002: Autosomal dominant mutilating keratoderma (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    358270018 Autosomal dominant mutilating keratoderma en Synonym Active Entire term case insensitive SNOMED CT core module
    628035017 Autosomal dominant mutilating keratoderma (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
    Autosomal dominant mutilating keratoderma Is a Mutilating keratoderma false Inferred relationship Existential restriction modifier
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Autosomal dominant mutilating keratoderma Associated morphology Hyperkeratosis false Inferred relationship Existential restriction modifier 2
    Autosomal dominant mutilating keratoderma Occurrence Congenital false Inferred relationship Existential restriction modifier
    Autosomal dominant mutilating keratoderma Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier
    Autosomal dominant mutilating keratoderma Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
    Autosomal dominant mutilating keratoderma Has definitional manifestation Abnormal keratinization false Inferred relationship Existential restriction modifier
    Autosomal dominant mutilating keratoderma Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Autosomal dominant mutilating keratoderma Occurrence Congenital false Inferred relationship Existential restriction modifier 3
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier 3
    Autosomal dominant mutilating keratoderma Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
    Autosomal dominant mutilating keratoderma Occurrence Congenital false Inferred relationship Existential restriction modifier 4
    Autosomal dominant mutilating keratoderma Associated morphology Hyperkeratosis false Inferred relationship Existential restriction modifier 4
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier 4
    Autosomal dominant mutilating keratoderma Has interpretation Abnormal false Inferred relationship Existential restriction modifier 1
    Autosomal dominant mutilating keratoderma Interprets Keratinization, function false Inferred relationship Existential restriction modifier 1
    Autosomal dominant mutilating keratoderma Finding site Skin structure of sole of foot false Inferred relationship Existential restriction modifier 3
    Autosomal dominant mutilating keratoderma Associated morphology Hyperkeratosis false Inferred relationship Existential restriction modifier 3
    Autosomal dominant mutilating keratoderma Finding site Skin structure of palmar area of hand false Inferred relationship Existential restriction modifier 2
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Keratoderma hereditarium mutilans with ichthyosis syndrome Is a False Autosomal dominant mutilating keratoderma Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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