Walker–Warburg syndrome (Q1629483)

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a rare form of autosomal recessive congenital muscular dystrophy.
  • Walker-Warburg syndrome
  • HARD syndrome
  • cerebroocular dysplasia-muscular dystrophy syndrome
  • Warburg syndrome
  • Chemke syndrome
  • Pagon syndrome
  • cerebroocular dysgenesis
  • cerebroocular dysplasia-muscular dystrophy syndrome (COD-MD)
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 1
  • MDDGA1
  • MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1
  • MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1
  • Cod-Md Syndrome
  • Hydrocephalus, Agyria, and Retinal Dysplasia
  • Walker-Warburg Syndrome or Muscle-Eye-Brain Disease, Pomt1-Related
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Language Label Description Also known as
English
Walker–Warburg syndrome
a rare form of autosomal recessive congenital muscular dystrophy.
  • Walker-Warburg syndrome
  • HARD syndrome
  • cerebroocular dysplasia-muscular dystrophy syndrome
  • Warburg syndrome
  • Chemke syndrome
  • Pagon syndrome
  • cerebroocular dysgenesis
  • cerebroocular dysplasia-muscular dystrophy syndrome (COD-MD)
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 1
  • MDDGA1
  • MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1
  • MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1
  • Cod-Md Syndrome
  • Hydrocephalus, Agyria, and Retinal Dysplasia
  • Walker-Warburg Syndrome or Muscle-Eye-Brain Disease, Pomt1-Related

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Identifiers

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MONDO:0009364
 
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