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239068002: Autosomal dominant mutilating keratoderma (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    358270018 Autosomal dominant mutilating keratoderma en Synonym Active Case insensitive SNOMED CT core
    628035017 Autosomal dominant mutilating keratoderma (disorder) en Fully specified name Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Autosomal dominant mutilating keratoderma Finding site Skin structure of sole of foot false Inferred relationship Some 3
    Autosomal dominant mutilating keratoderma Associated morphology Hyperkeratosis false Inferred relationship Some 3
    Autosomal dominant mutilating keratoderma Finding site Skin structure of palmar area of hand false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma Is a Autosomal dominant hereditary disorder false Inferred relationship Some
    Autosomal dominant mutilating keratoderma Is a Hereditary disorder of the integument false Inferred relationship Some
    Autosomal dominant mutilating keratoderma Has definitional manifestation Abnormal keratinisation false Inferred relationship Some
    Autosomal dominant mutilating keratoderma Associated morphology Congenital anomaly false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma Is a Mutilating keratoderma false Inferred relationship Some
    Autosomal dominant mutilating keratoderma Occurrence Congenital false Inferred relationship Some 3
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Some 3
    Autosomal dominant mutilating keratoderma Associated morphology Developmental abnormality false Inferred relationship Some 3
    Autosomal dominant mutilating keratoderma Occurrence Congenital false Inferred relationship Some 4
    Autosomal dominant mutilating keratoderma Associated morphology Hyperkeratosis false Inferred relationship Some 4
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Some 4
    Autosomal dominant mutilating keratoderma Has interpretation Abnormal false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma Interprets Keratinisation false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma Finding site Skin structure false Inferred relationship Some 1
    Autosomal dominant mutilating keratoderma Associated morphology Hyperkeratosis false Inferred relationship Some 2
    Autosomal dominant mutilating keratoderma Occurrence Congenital false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Keratoderma hereditarium mutilans with ichthyosis syndrome Is a False Autosomal dominant mutilating keratoderma Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set

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