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| Term | Charcot-Marie-Tooth disease type 4 | ID (Ontology) | DOID:0050541 (Human Disease) |
| Definition | A Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has_material_basis_in autosomal recessive inheritance. | ||
| Also Known As | "hereditary motor and sensory neuropathy" | ||
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neuromuscular disease |__Charcot-Marie-Tooth disease |__Charcot-Marie-Tooth disease type 4 39 rec. |__autosomal recessive axonal Charcot-Marie-Tooth disease with vocal cord paresis 1 rec. |__Charcot-Marie-Tooth disease type 4A 2 rec. |__Charcot-Marie-Tooth disease type 4B1 24 rec. |__Charcot-Marie-Tooth disease type 4B2 1 rec. |__Charcot-Marie-Tooth disease type 4B3 1 rec. |__Charcot-Marie-Tooth disease type 4C |__Charcot-Marie-Tooth disease type 4D 2 rec. |__Charcot-Marie-Tooth disease type 4E 1 rec. |__Charcot-Marie-Tooth disease type 4F |__Charcot-Marie-Tooth disease type 4G 1 rec. |__Charcot-Marie-Tooth disease type 4H 1 rec. |__Charcot-Marie-Tooth disease type 4J 6 rec. |__Charcot-Marie-Tooth disease type 4K 1 rec. |
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| Is a | Charcot-Marie-Tooth disease | ||
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GARD:12440 ORDO:64749 |
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