FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

59078009: Klippel-Trenaunay-Weber syndrome (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    98177018 Klippel-Trenaunay-Weber syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    98178011 Cerebrofacial angiomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    797880014 Klippel-Trenaunay-Weber syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    1216776014 Haemangiectatic hypertrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1218264016 Hemangiectatic hypertrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    98177018 Klippel-Trenaunay-Weber syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    98178011 Cerebrofacial angiomatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    98178011 Cerebrofacial angiomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    797880014 Klippel-Trenaunay-Weber syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    797880014 Klippel-Trenaunay-Weber syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    1216776014 Haemangiectatic hypertrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1216776014 Haemangiectatic hypertrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1218264016 Hemangiectatic hypertrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1218264016 Hemangiectatic hypertrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    107931000077115 angiodysplasie ostéodystrophique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    107931000077115 angiodysplasie ostéodystrophique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    angiodysplasie ostéodystrophique Is a Congenital anomaly of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Is a Multisystem disorder K-L (navigational concept) false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Is a Venous-lymphatic malformation false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Is a Hamartomatous disease false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Is a Congenital anomaly of integument false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    angiodysplasie ostéodystrophique Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Finding site Venous structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    angiodysplasie ostéodystrophique Finding site Cardiovascular system subdivision false Inferred relationship Existential restriction modifier (core metadata concept) 2
    angiodysplasie ostéodystrophique Finding site Structure of lymphoreticular system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Finding site Structure of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Is a trouble multisytémique false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Is a Congenital anomaly of skin (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Finding site Blood vessel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    angiodysplasie ostéodystrophique Is a Site-specific disorder of skin false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Is a Congenital arteriovenous malformation false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Is a Vascular hamartomas false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Associated morphology Arteriovenous malformation false Inferred relationship Existential restriction modifier (core metadata concept) 2
    angiodysplasie ostéodystrophique Finding site Arterial structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    angiodysplasie ostéodystrophique Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 2
    angiodysplasie ostéodystrophique Is a Congenital abnormality of vein false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Is a Disorder of musculoskeletal system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Finding site Blood vessel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    angiodysplasie ostéodystrophique Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    angiodysplasie ostéodystrophique Is a Haemangioma false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Is a Congenital connective tissue disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Is a Congenital malformation syndromes involving limbs false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Is a Hypertrophy of bone (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 2
    angiodysplasie ostéodystrophique Finding site Musculoskeletal structure of limb (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    angiodysplasie ostéodystrophique Associated morphology Hemangioma - category false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Associated morphology Hypertrophy of bone false Inferred relationship Existential restriction modifier (core metadata concept) 1
    angiodysplasie ostéodystrophique Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    angiodysplasie ostéodystrophique Associated morphology Hypertrophy of bone false Inferred relationship Existential restriction modifier (core metadata concept) 1
    angiodysplasie ostéodystrophique Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    angiodysplasie ostéodystrophique Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 2
    angiodysplasie ostéodystrophique Finding site Musculoskeletal structure of limb (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    angiodysplasie ostéodystrophique Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Finding site Blood vessel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Is a Hereditary dysplasia of blood vessel (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    angiodysplasie ostéodystrophique Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    angiodysplasie ostéodystrophique Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
    angiodysplasie ostéodystrophique Finding site Musculoskeletal structure of limb (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    REPLACED BY association reference set (foundation metadata concept)

    Back to Start