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| Term | autosomal dominant distal hereditary motor neuronopathy 6 | ID (Ontology) | DOID:0111210 (Human Disease) |
| Definition | A distal hereditary motor neuropathy that has_material_basis_in heterozygous mutation in the FBXO38 gene on 5q32. | ||
| Also Known As | "distal hereditary motor neuronopathy type 2D" ; "distal hereditary motor neuropathy type IID" ; "distal spinal muscular atrophy with calf predominance" (for all, see Synonyms field below) | ||
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autosomal dominant disease__ spinal muscular atrophy_____| autosomal dominant distal hereditary motor neuronopathy |__autosomal dominant distal hereditary motor neuronopathy 6 |
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| Is a | autosomal dominant distal hereditary motor neuronopathy | ||
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| MIM:615575 | |||