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| Term | infantile-onset distal myopathy | ID (Ontology) | DOID:0070196 (Human Disease) |
| Definition | A distal myopathy that is characterized by autosomal dominant inheritance, infantile onset and progressive disease development. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal dominant disease__ muscular dystrophy | |__distal myopathy_____________| infantile-onset distal myopathy |
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| Parents/Children View Depth |
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| Is a |
autosomal dominant disease distal myopathy |
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External Crossreferences & Linkouts
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| MIM:160300 | |||