FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

278841002: Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I (disorder)


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

    Descriptions:

    Id Description Lang Type Status Case? Module
    415859016 Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    672048012 Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    851661000052114 pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Is a Acromesomelic dysplasia syndrome false Inferred relationship Some
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Is a Pseudohypoparathyroidism and pseudopseudohypoparathyroidism false Inferred relationship Some
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Finding site Bone structure false Inferred relationship Some 1
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Associated morphology Dysplasia false Inferred relationship Some 1
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Finding site Structure of endocrine system (body structure) false Inferred relationship Some 2
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Occurrence Congenital false Inferred relationship Some
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Finding site Skeletal system structure false Inferred relationship Some 1
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Finding site Musculoskeletal structure of limb false Inferred relationship Some
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Is a Congenital anomaly of endocrine gland false Inferred relationship Some
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Associated morphology kongenital dysplasi false Inferred relationship Some 1
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Is a Metabolic bone disease false Inferred relationship Some
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Associated morphology kongenital dysplasi false Inferred relationship Some 1
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Finding site Bone structure false Inferred relationship Some 1
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Occurrence Congenital false Inferred relationship Some 2
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Finding site Bone structure false Inferred relationship Some 2
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Associated morphology kongenital dysplasi false Inferred relationship Some 2
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Occurrence Congenital false Inferred relationship Some 1
    pseudohypoparatyreoidism och pseudopseudohypoparatyreoidism, typ 1 Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    US English

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

    Back to Start