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| Term | Charcot-Marie-Tooth disease X-linked recessive 2 | ID (Ontology) | DOID:0110208 (Human Disease) |
| Definition | A Charcot-Marie-Tooth disease X-linked that has_material_basis_in variation in the region Xp22.2. | ||
| Also Known As | "Charcot-Marie-Tooth neuropathy X-linked recessive 2" ; "CMTX2" ; "X-linked Charcot-Marie-Tooth disease type 2" | ||
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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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X-linked monogenic disease |__X-linked recessive disease__________ Charcot-Marie-Tooth disease | |__Charcot-Marie-Tooth disease type X__| Charcot-Marie-Tooth disease X-linked recessive 2 |
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| Is a |
Charcot-Marie-Tooth disease type X X-linked recessive disease |
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ICD10CM:G60.0 MESH:C535302 MIM:302801 ORDO:101076 |
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