FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

59078009: Klippel-Trenaunay-Weber syndrome (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    98177018 Klippel-Trenaunay-Weber syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
    98178011 Cerebrofacial angiomatosis en Synonym Active Entire term case insensitive SNOMED CT core module
    797880014 Klippel-Trenaunay-Weber syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
    1216776014 Haemangiectatic hypertrophy en Synonym Active Entire term case insensitive SNOMED CT core module
    1218264016 Hemangiectatic hypertrophy en Synonym Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Klippel-Trenaunay-Weber syndrome Is a Congenital anomaly of musculoskeletal system false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Is a Multisystem disorder K-L false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Is a Venous-lymphatic malformation false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Is a Congenital hamartosis false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Is a Congenital anomaly of integument false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Klippel-Trenaunay-Weber syndrome Finding site Structure of skin region false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Finding site Venous structure false Inferred relationship Existential restriction modifier 1
    Klippel-Trenaunay-Weber syndrome Finding site Structure of cardiovascular system subdivision false Inferred relationship Existential restriction modifier 2
    Klippel-Trenaunay-Weber syndrome Finding site Structure of lymphoreticular system false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Finding site Structure of musculoskeletal system false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Is a Multisystem disorder false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Is a Congenital anomaly of skin false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Finding site Blood vessel structure false Inferred relationship Existential restriction modifier 1
    Klippel-Trenaunay-Weber syndrome Is a Site-specific disorder of skin false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Is a Congenital arteriovenous malformation false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Is a Vascular hamartomas false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Associated morphology Arteriovenous malformation false Inferred relationship Existential restriction modifier 2
    Klippel-Trenaunay-Weber syndrome Finding site Arterial structure false Inferred relationship Existential restriction modifier 2
    Klippel-Trenaunay-Weber syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 2
    Klippel-Trenaunay-Weber syndrome Is a Congenital abnormality of vein false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Is a Disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Finding site Blood vessel structure false Inferred relationship Existential restriction modifier 2
    Klippel-Trenaunay-Weber syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Klippel-Trenaunay-Weber syndrome Is a Hemangioma false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Is a Congenital connective tissue disorder false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Is a Congenital malformation syndromes involving limbs false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Is a Hypertrophy of bone false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 2
    Klippel-Trenaunay-Weber syndrome Finding site Musculoskeletal structure of limb false Inferred relationship Existential restriction modifier 2
    Klippel-Trenaunay-Weber syndrome Associated morphology Hemangioma - category false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Associated morphology Hypertrophy of bone false Inferred relationship Existential restriction modifier 1
    Klippel-Trenaunay-Weber syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 1
    Klippel-Trenaunay-Weber syndrome Associated morphology Hypertrophy of bone false Inferred relationship Existential restriction modifier 1
    Klippel-Trenaunay-Weber syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 1
    Klippel-Trenaunay-Weber syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 2
    Klippel-Trenaunay-Weber syndrome Finding site Musculoskeletal structure of limb false Inferred relationship Existential restriction modifier 2
    Klippel-Trenaunay-Weber syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Finding site Blood vessel structure false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Is a Hereditary dysplasia of blood vessel false Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Klippel-Trenaunay-Weber syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
    Klippel-Trenaunay-Weber syndrome Finding site Musculoskeletal structure of limb false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

    Back to Start