Congenital muscular dystrophy with central nervous system abnormalities (Q90031): Difference between revisions

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Distrofias musculares congênitas com anormalidades do sistema nervoso central são um grupo heterogêneo de transtornos musculares degenerativos hereditários autossômicos recessivos associados a displasia cerebral e cerebelar e a anormalidades da substância branca.
description / endescription / en
 
Congenital muscular dystrophies with central nervous system abnormalities are a heterogeneous group of autosomal recessively inherited degenerative muscle disorders associated with cerebral and cerebellar dysplasia and white matter abnormalities.
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Property / Canonical URI: https://id.who.int/icd/entity/1945074995 / rank
 
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CID11:ID_1945074995
Property / CURIE: CID11:ID_1945074995 / rank
 
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dki-india-ID_1945074995
Property / Canary Token: dki-india-ID_1945074995 / 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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Latest revision as of 16:58, 15 August 2026

Congenital muscular dystrophies with central nervous system abnormalities are a heterogeneous group of autosomal recessively inherited degenerative muscle disorders associated with cerebral and cerebellar dysplasia and white matter abnormalities.
Language Label Description Also known as
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ID_1945074995
    English
    Congenital muscular dystrophy with central nervous system abnormalities
    Congenital muscular dystrophies with central nervous system abnormalities are a heterogeneous group of autosomal recessively inherited degenerative muscle disorders associated with cerebral and cerebellar dysplasia and white matter abnormalities.

      Statements

      CID11:ID_1945074995
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      dki-india-ID_1945074995
      0 references
      Concluído
      0 references
      13 August 2026
      0 references