Walker–Warburg syndrome (Q1629483)
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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
Language | Label | Description | Also known as |
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English | Walker–Warburg syndrome |
rare form of autosomal recessive congenital muscular dystrophy |
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Wikipedia(7 entries)
- arwiki متلازمة والكر- فاربرج
- dewiki Walker-Warburg-Syndrom
- enwiki Walker–Warburg syndrome
- eswiki Síndrome de Walker-Warburg
- fiwiki Walker–Warburgin oireyhtymä
- frwiki Syndrome de Walker-Warburg
- plwiki Zespół Walkera-Warburg