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47063001: Hereditary vitamin D dependency syndrome type, II (disorder)

    Status: retired, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    494745015 Hereditary generalised resistance to 1 alpha, 25(OH)>2< D en Synonym Active Initial character case insensitive SNOMED CT core
    78444018 Hereditary vitamin D dependency syndrome type, II en Synonym Active Initial character case insensitive SNOMED CT core
    78445017 Hereditary generalized resistance to 1 alpha, 25(OH)>2< D en Synonym Active Initial character case insensitive SNOMED CT core
    78446016 ARUDD-II en Synonym Active Case sensitive SNOMED CT core
    784480014 Hereditary vitamin D dependency syndrome type, II (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Hereditary vitamin D dependency syndrome type, II Finding site Structure of endocrine system false Inferred relationship Some
    Hereditary vitamin D dependency syndrome type, II Is a Hereditary vitamin D dependency syndrome false Inferred relationship Some
    Hereditary vitamin D dependency syndrome type, II Occurrence Congenital false Inferred relationship Some 1
    Hereditary vitamin D dependency syndrome type, II Finding site Structure of endocrine system false Inferred relationship Some 1
    Hereditary vitamin D dependency syndrome type, II Finding site Entire endocrine gonad false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

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