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| Term | congenital muscular dystrophy-dystroglycanopathy type A10 | ID (Ontology) | DOID:0111239 (Human Disease) |
| Definition | A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in RXYLT1 on 12q14.2. | ||
| Also Known As | "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A10" ; "MDDGA10" ; "Walker-Warburg syndrome or muscle-eye-brain disease, TMEM5-related" | ||
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| DO.org | |||
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autosomal recessive disease____________ muscular dystrophy-dystroglycanopathy__| congenital muscular dystrophy-dystroglycanopathy type A |__congenital muscular dystrophy-dystroglycanopathy type A10 |
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| Is a | congenital muscular dystrophy-dystroglycanopathy type A | ||
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| MIM:615041 | |||