Ehlers-Danlos syndrome, dysfibronectinaemic type (Q101861): Difference between revisions
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A síndrome de Ehlers-Danlos, tipo fibronectinêmico é um tipo de síndrome de Ehlers-Danlos (SED), um grupo heterogêneo de doenças hereditárias do tecido conjuntivo caracterizadas por hipermobilidade articular variável e hiperextensibilidade cutânea e que se distingue pela disfunção plaquetária associada a uma anormalidade da fibronectina. | |||||||||||||||
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Ehlers-Danlos syndrome, fibronectinemic type is a type of Ehlers-Danlos syndromes (EDS), a heterogeneous group of inherited connective tissue disorders characterised by variable joint hypermobility and cutaneous hyperextensibility and is distinguished by platelet dysfunction associated with a fibronectin abnormality. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1014914201 / rank | |||||||||||||||
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CID11:ID_1014914201 | |||||||||||||||
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dki-india-ID_1014914201 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest revision as of 18:42, 16 August 2026
Ehlers-Danlos syndrome, fibronectinemic type is a type of Ehlers-Danlos syndromes (EDS), a heterogeneous group of inherited connective tissue disorders characterised by variable joint hypermobility and cutaneous hyperextensibility and is distinguished by platelet dysfunction associated with a fibronectin abnormality.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1014914201 |
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| English | Ehlers-Danlos syndrome, dysfibronectinaemic type |
Ehlers-Danlos syndrome, fibronectinemic type is a type of Ehlers-Danlos syndromes (EDS), a heterogeneous group of inherited connective tissue disorders characterised by variable joint hypermobility and cutaneous hyperextensibility and is distinguished by platelet dysfunction associated with a fibronectin abnormality. |
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CID11:ID_1014914201
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dki-india-ID_1014914201
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Concluído
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15 August 2026
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