Chondrocalcinosis (Q44294): Difference between revisions

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A condrocalcinose refere-se à calcificação radiográfica das estruturas fibrocartilaginosas e/ou cartilagem hialina e não é específica para DPFC ou outra doença por deposição de cristais. Nos diversos países em que doença por deposição de pirofosfato de cálcio familiar l (DPFC Familiar l ) foi descrita, alguns indivíduos com o mesmo grau de parentesco tiveram a DPFC associada à mutação ANKH no cromossomo 5p.
description / endescription / en
 
Chondrocalcinosis refers to radiographic calcification in hyaline and/or fibrocartilage and is not specific for CPPD or other particular crystal deposition disease. Familial l CPPD deposition disease has been reported from many countries and some kindred have CPPD disease linked to ANKH mutation on chromosome 5p.
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Property / Canonical URI: https://id.who.int/icd/entity/2041797033 / rank
 
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CID11:FA26.2
Property / CURIE: CID11:FA26.2 / rank
 
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dki-india-FA26.2
Property / Canary Token: dki-india-FA26.2 / rank
 
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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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13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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Property / Linked ICD 10: M11.2 / rank
 
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Latest revision as of 11:42, 13 August 2026

Chondrocalcinosis refers to radiographic calcification in hyaline and/or fibrocartilage and is not specific for CPPD or other particular crystal deposition disease. Familial l CPPD deposition disease has been reported from many countries and some kindred have CPPD disease linked to ANKH mutation on chromosome 5p.
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FA26.2
    English
    Chondrocalcinosis
    Chondrocalcinosis refers to radiographic calcification in hyaline and/or fibrocartilage and is not specific for CPPD or other particular crystal deposition disease. Familial l CPPD deposition disease has been reported from many countries and some kindred have CPPD disease linked to ANKH mutation on chromosome 5p.

      Statements

      CID11:FA26.2
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      dki-india-FA26.2
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      Concluído
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      13 August 2026
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