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61165007: Hereditary nephrogenic diabetes insipidus (disorder)


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

    Descriptions:

    Id Description Lang Type Status Case? Module
    101638011 Hereditary nephrogenic diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    101640018 Familial nephrogenic diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    101641019 Vasopressin-unresponsiveness hyposthenuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    101642014 Vasopressin-resistant diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    101643016 ADH-resistant diabetes insipidus en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    101644010 Adiuretin-resistant diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    101645011 Renal diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    101646012 Vasopressin-resistant hyposthenuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    498950010 Congenital nephrogenic diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    498951014 Primary nephrogenic diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    800197017 Hereditary nephrogenic diabetes insipidus (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    101638011 Hereditary nephrogenic diabetes insipidus en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    101638011 Hereditary nephrogenic diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    101640018 Familial nephrogenic diabetes insipidus en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    101640018 Familial nephrogenic diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    101641019 Vasopressin-unresponsiveness hyposthenuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    101641019 Vasopressin-unresponsiveness hyposthenuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    101642014 Vasopressin-resistant diabetes insipidus en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    101642014 Vasopressin-resistant diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    101643016 ADH-resistant diabetes insipidus en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    101644010 Adiuretin-resistant diabetes insipidus en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    101644010 Adiuretin-resistant diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    101645011 Renal diabetes insipidus en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    101645011 Renal diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    101646012 Vasopressin-resistant hyposthenuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    101646012 Vasopressin-resistant hyposthenuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    498950010 Congenital nephrogenic diabetes insipidus en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    498950010 Congenital nephrogenic diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    498951014 Primary nephrogenic diabetes insipidus en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    498951014 Primary nephrogenic diabetes insipidus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    800197017 Hereditary nephrogenic diabetes insipidus (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    800197017 Hereditary nephrogenic diabetes insipidus (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    4590691000241110 diabète insipide néphrogénique héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    4590691000241110 diabète insipide néphrogénique héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    diabète insipide néphrogénique héréditaire Is a Hereditary disorder of endocrine system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Is a Arginine vasopressin resistance (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Is a Familial vasopressin-related polyuria false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Is a Reproductive system hereditary disorder (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Is a Hereditary disorder of the urinary system false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Is a Inflammatory disorder of head false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Finding site Neurohypophysis structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Finding site Structure of interstitial tissue of kidney false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Interprets Nutritional deficiency state false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Finding site Renal tubule structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Is a Hereditary nephropathy (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    diabète insipide néphrogénique héréditaire Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    diabète insipide néphrogénique héréditaire Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    diabète insipide néphrogénique héréditaire Finding site Neurohypophysis structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    diabète insipide néphrogénique héréditaire Finding site Renal tubule structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    diabète insipide néphrogénique héréditaire Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)

    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)

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