Bleeding diathesis due to integrin alpha2-beta1 deficiency (Q100852): Difference between revisions

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Susceptibilidade incomum a sangramento (hemorragia) majoritariamente devida a hipocoagulabilidade, por sua vez causada por uma coagulopatia (um defeito no sistema da coagulação). Este diagnóstico é devido a uma deficiência nos receptores transmembrana que mediam a ligação entre a célula e os tecidos que a cercam, como as outras células e a matriz extracelular (MEC).
description / endescription / en
 
This is an unusual susceptibility to bleeding (haemorrhage) mostly due to hypocoagulability, in turn caused by a coagulopathy (a defect in the system of coagulation). This diagnosis is due to a deficiency in the transmembrane receptors that mediate the attachment between a cell and the tissues that surround it, such as other cells or the extracellular matrix (ECM).
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1508140529 / rank
 
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Property / CURIE
 
CID11:ID_1508140529
Property / CURIE: CID11:ID_1508140529 / rank
 
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Property / Canary Token
 
dki-india-ID_1508140529
Property / Canary Token: dki-india-ID_1508140529 / 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 17:37, 16 August 2026

This is an unusual susceptibility to bleeding (haemorrhage) mostly due to hypocoagulability, in turn caused by a coagulopathy (a defect in the system of coagulation). This diagnosis is due to a deficiency in the transmembrane receptors that mediate the attachment between a cell and the tissues that surround it, such as other cells or the extracellular matrix (ECM).
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ID_1508140529
    English
    Bleeding diathesis due to integrin alpha2-beta1 deficiency
    This is an unusual susceptibility to bleeding (haemorrhage) mostly due to hypocoagulability, in turn caused by a coagulopathy (a defect in the system of coagulation). This diagnosis is due to a deficiency in the transmembrane receptors that mediate the attachment between a cell and the tissues that surround it, such as other cells or the extracellular matrix (ECM).

      Statements

      CID11:ID_1508140529
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      dki-india-ID_1508140529
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      Concluído
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      15 August 2026
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