FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

239068002: autosomaal dominante keratoderma hereditarium mutilans (aandoening)

    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
    6352571000146114 autosomaal dominante keratoderma hereditarium mutilans nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    6352581000146111 autosomaal dominante keratoderma hereditarium mutilans (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    6352591000146113 mutilerende keratodermie van Vohwinkel nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    6352611000146118 syndroom van Vohwinkel nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    6352621000146111 Vohwinkel-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    autosomaal dominante keratoderma hereditarium mutilans Is a Mutilating keratoderma false Inferred relationship Some
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure false Inferred relationship Some 1
    autosomaal dominante keratoderma hereditarium mutilans Associated morphology Hyperkeratosis false Inferred relationship Some 2
    autosomaal dominante keratoderma hereditarium mutilans Occurrence Congenital false Inferred relationship Some
    autosomaal dominante keratoderma hereditarium mutilans Is a Autosomal dominant hereditary disorder false Inferred relationship Some
    autosomaal dominante keratoderma hereditarium mutilans Is a Hereditary disorder of the integument false Inferred relationship Some
    autosomaal dominante keratoderma hereditarium mutilans Has definitional manifestation Abnormal keratinization false Inferred relationship Some
    autosomaal dominante keratoderma hereditarium mutilans Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 1
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure false Inferred relationship Some 2
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure false Inferred relationship Some 1
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure false Inferred relationship Some 2
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure false Inferred relationship Some 2
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure false Inferred relationship Some 1
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure false Inferred relationship Some 1
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure false Inferred relationship Some 2
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure false Inferred relationship Some 1
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure false Inferred relationship Some 2
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure false Inferred relationship Some 1
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure false Inferred relationship Some 2
    autosomaal dominante keratoderma hereditarium mutilans Occurrence Congenital false Inferred relationship Some 3
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure false Inferred relationship Some 3
    autosomaal dominante keratoderma hereditarium mutilans Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 3
    autosomaal dominante keratoderma hereditarium mutilans Occurrence Congenital false Inferred relationship Some 4
    autosomaal dominante keratoderma hereditarium mutilans Associated morphology Hyperkeratosis false Inferred relationship Some 4
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure false Inferred relationship Some 4
    autosomaal dominante keratoderma hereditarium mutilans Has interpretation Abnormal false Inferred relationship Some 1
    autosomaal dominante keratoderma hereditarium mutilans Interprets Keratinization false Inferred relationship Some 1
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure of sole of foot (body structure) false Inferred relationship Some 3
    autosomaal dominante keratoderma hereditarium mutilans Associated morphology Hyperkeratosis false Inferred relationship Some 3
    autosomaal dominante keratoderma hereditarium mutilans Finding site Skin structure of palmar area of hand false Inferred relationship Some 2
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) Is a False autosomaal dominante keratoderma hereditarium mutilans Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

    Back to Start