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46011003: Ruvalcaba-Myhre syndrome (disorder)

    Status: retired, Primitive. Date: 31-Jul 2020. Module: SNOMED CT core

    Descriptions:

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

    0 descendants.

    Expanded Value Set

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

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set

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