Hyperphosphataemic familial tumoural calcinosis (Q97254): Difference between revisions

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description / pt-brdescription / pt-br
 
Distúrbio eletrolítico no qual há um nível anormalmente alto de fosfato no sangue, em uma condição rara em que há deposição de cálcio no tecido mole na localização periarticular, ou seja, ao redor das articulações.
description / endescription / en
 
This is an electrolyte disturbance in which there is an abnormally low level of phosphate in the blood, in a rare condition in which there is calcium deposition in the soft tissue in periarticular location i.e. around joints.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/20891450 / rank
 
Normal rank
Property / CURIE
 
CID11:ID_20891450
Property / CURIE: CID11:ID_20891450 / rank
 
Normal rank
Property / Canary Token
 
dki-india-ID_20891450
Property / Canary Token: dki-india-ID_20891450 / rank
 
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Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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Property / Collection date
 
15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 13:20, 16 August 2026

This is an electrolyte disturbance in which there is an abnormally low level of phosphate in the blood, in a rare condition in which there is calcium deposition in the soft tissue in periarticular location i.e. around joints.
Language Label Description Also known as
default for all languages
ID_20891450
    English
    Hyperphosphataemic familial tumoural calcinosis
    This is an electrolyte disturbance in which there is an abnormally low level of phosphate in the blood, in a rare condition in which there is calcium deposition in the soft tissue in periarticular location i.e. around joints.

      Statements

      CID11:ID_20891450
      0 references
      dki-india-ID_20891450
      0 references
      Concluído
      0 references
      15 August 2026
      0 references