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46011003: Ruvalcaba-Myhre syndrome (disorder)

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

    Descriptions:

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

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Ruvalcaba-Myhre syndrome Is a Ruvalcaba syndrome false Inferred relationship Existential restriction modifier
    Ruvalcaba-Myhre syndrome Is a Congenital hamartosis false Inferred relationship Existential restriction modifier
    Ruvalcaba-Myhre syndrome Finding site Musculoskeletal structure of limb false Inferred relationship Existential restriction modifier
    Ruvalcaba-Myhre syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
    Ruvalcaba-Myhre syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier
    Ruvalcaba-Myhre syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Ruvalcaba-Myhre syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier 1
    Ruvalcaba-Myhre syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier
    Ruvalcaba-Myhre syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
    Ruvalcaba-Myhre syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier 1
    Ruvalcaba-Myhre syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
    Ruvalcaba-Myhre syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Ruvalcaba-Myhre syndrome Is a Congenital hamartoma false Inferred relationship Existential restriction modifier
    Ruvalcaba-Myhre syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier 2
    Ruvalcaba-Myhre syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
    Ruvalcaba-Myhre syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
    Ruvalcaba-Myhre syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 2
    Ruvalcaba-Myhre syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
    Ruvalcaba-Myhre syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier 3
    Ruvalcaba-Myhre syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
    Ruvalcaba-Myhre syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier 4
    Ruvalcaba-Myhre syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 3
    Ruvalcaba-Myhre syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 3
    Ruvalcaba-Myhre syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 3
    Ruvalcaba-Myhre syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Ruvalcaba-Myhre syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
    Ruvalcaba-Myhre syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Ruvalcaba-Myhre syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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