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237657009: Hypoparathyroidism - autosomal dominant (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2022. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    356189019 Hypoparathyroidism - autosomal dominant en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    626417013 Hypoparathyroidism - autosomal dominant (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    356189019 Hypoparathyroidism - autosomal dominant en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    356189019 Hypoparathyroidism - autosomal dominant en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    626417013 Hypoparathyroidism - autosomal dominant (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    626417013 Hypoparathyroidism - autosomal dominant (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Hypoparathyroidism - autosomal dominant Is a Hypoparathyroidism false Inferred relationship Existential restriction modifier (core metadata concept)
    Hypoparathyroidism - autosomal dominant Finding site Parathyroid structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Hypoparathyroidism - autosomal dominant Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    Hypoparathyroidism - autosomal dominant Interprets Nutritional deficiency state false Inferred relationship Existential restriction modifier (core metadata concept)
    Hypoparathyroidism - autosomal dominant Has definitional manifestation Decreased hormone secretion false Inferred relationship Existential restriction modifier (core metadata concept)
    Hypoparathyroidism - autosomal dominant Has interpretation Decreased false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hypoparathyroidism - autosomal dominant Interprets Hormone secretion 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)

    REPLACED BY association reference set (foundation metadata concept)

    SAME AS association reference set (foundation metadata concept)

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