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1217517004: Autosomal recessive familial isolated hypoparathyroidism (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Nov 2024. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    5036557019 Autosomal recessive familial isolated hypoparathyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    5036558012 Autosomal recessive familial isolated hypoparathyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    5036557019 Autosomal recessive familial isolated hypoparathyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    5036558012 Autosomal recessive familial isolated hypoparathyroidism en Synonym (core metadata concept) 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
    Autosomal recessive familial isolated hypoparathyroidism Is a A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism causing hypocalcemia due to insufficient serum levels of bioactive parathormone (PTH), without other endocrine disorders or developmental defects. false Inferred relationship Existential restriction modifier (core metadata concept)
    Autosomal recessive familial isolated hypoparathyroidism Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    Autosomal recessive familial isolated hypoparathyroidism Finding site Parathyroid structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Autosomal recessive familial isolated hypoparathyroidism Interprets Hormone secretion false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Autosomal recessive familial isolated hypoparathyroidism Has interpretation Decreased 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)

    POSSIBLY EQUIVALENT TO association reference set

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