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278841002: Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    415859016 Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I en Synonym Active Initial character case insensitive SNOMED CT core
    672048012 Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I (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
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Occurrence Congenital false Inferred relationship Some 1
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Pathological process Pathological developmental process false Inferred relationship Some 1
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Is a Congenital anomaly of endocrine gland false Inferred relationship Some
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Associated morphology Congenital dysplasia false Inferred relationship Some 1
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Is a Metabolic bone disease false Inferred relationship Some
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Associated morphology Congenital dysplasia false Inferred relationship Some 1
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Finding site Bone structure false Inferred relationship Some 1
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Occurrence Congenital false Inferred relationship Some 2
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Finding site Bone structure false Inferred relationship Some 2
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Associated morphology Congenital dysplasia false Inferred relationship Some 2
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Finding site Bone structure false Inferred relationship Some 1
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Associated morphology Dysplasia false Inferred relationship Some 1
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Finding site Structure of endocrine system false Inferred relationship Some 2
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Occurrence Congenital false Inferred relationship Some
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Finding site Skeletal system structure false Inferred relationship Some 1
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Finding site Musculoskeletal structure of limb false Inferred relationship Some
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Is a Acromesomelic dysplasia syndrome false Inferred relationship Some
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Is a Pseudohypoparathyroidism and pseudopseudohypoparathyroidism false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Australian dialect reference set

    Concept inactivation indicator reference set

    Description inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

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