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| Term | Charcot-Marie-Tooth disease type 1F | ID (Ontology) | DOID:0110149 (Human Disease) |
| Definition | A Charcot-Marie-Tooth disease type 1 that has_material_basis_in mutation in the NEFL gene. | ||
| Also Known As | "Charcot-Marie-Tooth neuropathy type 1F" ; "CMT1F" | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease__________ |__autosomal recessive disease_________| Charcot-Marie-Tooth disease | |__Charcot-Marie-Tooth disease type 1__| Charcot-Marie-Tooth disease type 1F |
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| Is a |
Charcot-Marie-Tooth disease type 1 autosomal dominant disease autosomal recessive disease |
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External Crossreferences & Linkouts
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ICD10CM:G60.0 MIM:607734 ORDO:101085 |
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