Autosomal dominant spastic paraplegia type 29 (Q100930): Difference between revisions

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Property / Canonical URI: https://id.who.int/icd/entity/1125341564 / rank
 
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CID11:ID_1125341564
Property / CURIE: CID11:ID_1125341564 / rank
 
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dki-india-ID_1125341564
Property / Canary Token: dki-india-ID_1125341564 / 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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15 August 2026
Timestamp+2026-08-15T00:00:00Z
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CalendarGregorian
Precision1 day
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Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 17:43, 16 August 2026

Autosomal dominant spastic paraplegia characterized by spastic paraplegia presenting in adolescence along with sensorineural hearing impairment due to auditory neuropathy and persistent vomiting due to a hiatal or paraesophageal hernia.
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ID_1125341564
    English
    Autosomal dominant spastic paraplegia type 29
    Autosomal dominant spastic paraplegia characterized by spastic paraplegia presenting in adolescence along with sensorineural hearing impairment due to auditory neuropathy and persistent vomiting due to a hiatal or paraesophageal hernia.

      Statements

      CID11:ID_1125341564
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      dki-india-ID_1125341564
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      Concluído
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      15 August 2026
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