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| Term | Charcot-Marie-Tooth disease dominant intermediate G | ID (Ontology) | DOID:0080294 (Human Disease) |
| Definition | A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in heterozygous mutation in the NEFL gene on chromosome 8p21. | ||
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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_____________________ Charcot-Marie-Tooth disease | |__Charcot-Marie-Tooth disease intermediate type__| Charcot-Marie-Tooth disease dominant intermediate G |
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| Is a |
Charcot-Marie-Tooth disease intermediate type autosomal dominant disease |
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External Crossreferences & Linkouts
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| MIM:617882 | |||