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

46011003: Ruvalcaba-Myhre syndrome (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    76706017 Ruvalcaba-Myhre syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    494409019 Haemangiomata with macrocephaly and pseudopapilloedema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    494410012 Hemangiomata with macrocephaly and pseudopapilledema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    783314019 Ruvalcaba-Myhre syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3035444016 Ruvalcaba Myhre Smith syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    76706017 Ruvalcaba-Myhre syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    494409019 Haemangiomata with macrocephaly and pseudopapilloedema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    494409019 Haemangiomata with macrocephaly and pseudopapilloedema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    494410012 Hemangiomata with macrocephaly and pseudopapilledema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    494410012 Hemangiomata with macrocephaly and pseudopapilledema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    783314019 Ruvalcaba-Myhre syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    783314019 Ruvalcaba-Myhre syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3035444016 Ruvalcaba Myhre Smith syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Ruvalcaba-Myhre syndrome Is a Ruvalcaba syndrome (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Ruvalcaba-Myhre syndrome Is a Hamartomatous disease false Inferred relationship Existential restriction modifier (core metadata concept)
    Ruvalcaba-Myhre syndrome Finding site Musculoskeletal structure of limb (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    Ruvalcaba-Myhre syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Ruvalcaba-Myhre syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept)
    Ruvalcaba-Myhre syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ruvalcaba-Myhre syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ruvalcaba-Myhre syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept)
    Ruvalcaba-Myhre syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ruvalcaba-Myhre syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ruvalcaba-Myhre syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ruvalcaba-Myhre syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Ruvalcaba-Myhre syndrome Is a Congenital hamartoma (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Ruvalcaba-Myhre syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Ruvalcaba-Myhre syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Ruvalcaba-Myhre syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Ruvalcaba-Myhre syndrome Finding site Face structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Ruvalcaba-Myhre syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Ruvalcaba-Myhre syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Ruvalcaba-Myhre syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
    Ruvalcaba-Myhre syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept) 4
    Ruvalcaba-Myhre syndrome Finding site Face structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Ruvalcaba-Myhre syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Ruvalcaba-Myhre syndrome Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Ruvalcaba-Myhre syndrome Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ruvalcaba-Myhre syndrome Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Ruvalcaba-Myhre syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Ruvalcaba-Myhre syndrome Associated morphology Morphologically abnormal 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)

    SAME AS association reference set (foundation metadata concept)

    Back to Start