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278841002: Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    415859016 Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I en Synonym Active Only initial character case insensitive SNOMED CT core module
    672048012 Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Is a Acromesomelic dysplasia group false Inferred relationship Existential restriction modifier
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Is a Pseudohypoparathyroidism and pseudopseudohypoparathyroidism false Inferred relationship Existential restriction modifier
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Finding site Bone structure false Inferred relationship Existential restriction modifier 1
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Associated morphology Dysplasia false Inferred relationship Existential restriction modifier 1
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Finding site Structure of endocrine system false Inferred relationship Existential restriction modifier 2
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Occurrence Congenital false Inferred relationship Existential restriction modifier
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Finding site Skeletal system structure false Inferred relationship Existential restriction modifier 1
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Finding site Musculoskeletal structure of limb false Inferred relationship Existential restriction modifier
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Is a Congenital anomaly of endocrine gland false Inferred relationship Existential restriction modifier
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Is a Metabolic bone disease false Inferred relationship Existential restriction modifier
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Finding site Bone structure false Inferred relationship Existential restriction modifier 1
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Finding site Bone structure false Inferred relationship Existential restriction modifier 2
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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