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239068002: Autosomal dominant mutilating keratoderma (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    358270018 Autosomal dominant mutilating keratoderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    628035017 Autosomal dominant mutilating keratoderma (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
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) Skin structure of sole of foot false Inferred relationship Some 3
    Autosomal dominant mutilating keratoderma morphologie associée (attribut) Hyperkeratosis false Inferred relationship Some 3
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) peau de la région palmaire de la main (structure corporelle) false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma est un(e) (attribut) Autosomal dominant hereditary disorder false Inferred relationship Some
    Autosomal dominant mutilating keratoderma est un(e) (attribut) Hereditary disorder of the integument false Inferred relationship Some
    Autosomal dominant mutilating keratoderma est défini par la manifestation de (attribut) Abnormal keratinisation false Inferred relationship Some
    Autosomal dominant mutilating keratoderma morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma est un(e) (attribut) Mutilating keratoderma false Inferred relationship Some
    Autosomal dominant mutilating keratoderma survenue (attribut) congénital false Inferred relationship Some 3
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 3
    Autosomal dominant mutilating keratoderma morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 3
    Autosomal dominant mutilating keratoderma survenue (attribut) congénital false Inferred relationship Some 4
    Autosomal dominant mutilating keratoderma morphologie associée (attribut) Hyperkeratosis false Inferred relationship Some 4
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 4
    Autosomal dominant mutilating keratoderma a pour interprétation (attribut) anormal false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma interprète (attribut) Keratinization, function (observable entity) false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma morphologie associée (attribut) Hyperkeratosis false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma survenue (attribut) congénital false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) est un(e) (attribut) False Autosomal dominant mutilating keratoderma Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

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