Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies), Type A, 3 (*)

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  2. Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies), Type A, 3 (*)

Alternative Names

  • MDDGA3
  • Walker-Warburg Syndrome or Muscle-Eye-Brain Disease, POMGNT1-Related

Associated Genes

Protein O-Mannosyltransferase 1
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WHO-ICD-10 version:2010

Congenital malformations, deformations and chromosomal abnormalities

Congenital malformations of the nervous system

OMIM Number

253280

Mode of Inheritance

Autosomal recessive

Gene Map Locus

1p34.1

Epidemiology in the Arab World

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Edit History

  • Pratibha Nair: 22.01.2015
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© CAGS 2024. All rights reserved.