Pelizaeus-Merzbacher disease (Q1876206): Difference between revisions

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Changed reference of claim: ICD-10-CM (P4229): E75.2, см. / see autofix на / on Property talk:P5270
Removed claim: WikiProjectMed ID (P11143): Pelizaeus–Merzbacher disease, дублирующееся значение / duplicate value
Tag: Manual revert
 
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Latest revision as of 07:51, 15 June 2024

hypomyelinating leukodystrophy characterized by impaired myelin formation, nystagmus, spastic quadriplegia, ataxia, and developmental delay that has material basis in mutation in the PLP1 gene on chromosome Xq22
  • Leukodystrophy, sudanophilic
  • Pelizaeus Merzbacher brain sclerosis
  • Pelizaeus-Merzbacher disease (disorder)
  • HLD1
  • PMD
  • Pelizaeus-Merzbacher brain sclerosis
  • diffuse familial brain sclerosis
  • hypomyelinating leukodystrophy 1
  • sudanophilic leukodystrophy, Paelizeus-Merzbacher type
  • PELIZAEUS-MERZBACHER DISEASE
  • PELIZAEUS-MERZBACHER DISEASE; PMD
  • Pelizaeus Merzbacher disease
  • Leukodystrophy, Hypomyelinating, 1
Language Label Description Also known as
English
Pelizaeus-Merzbacher disease
hypomyelinating leukodystrophy characterized by impaired myelin formation, nystagmus, spastic quadriplegia, ataxia, and developmental delay that has material basis in mutation in the PLP1 gene on chromosome Xq22
  • Leukodystrophy, sudanophilic
  • Pelizaeus Merzbacher brain sclerosis
  • Pelizaeus-Merzbacher disease (disorder)
  • HLD1
  • PMD
  • Pelizaeus-Merzbacher brain sclerosis
  • diffuse familial brain sclerosis
  • hypomyelinating leukodystrophy 1
  • sudanophilic leukodystrophy, Paelizeus-Merzbacher type
  • PELIZAEUS-MERZBACHER DISEASE
  • PELIZAEUS-MERZBACHER DISEASE; PMD
  • Pelizaeus Merzbacher disease
  • Leukodystrophy, Hypomyelinating, 1

Statements

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Identifiers

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8A44.0
Pelizaeus-Merzbacher disease
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