WormBase Tree Display for DO_term: DOID:0110175
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| DOID:0110175 | Name | Charcot-Marie-Tooth disease axonal type 2O | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the DYNC1H1 gene on chromosome 14q32. | ||||
| Synonym | Exact | Charcot-Marie-Tooth neuropathy axonal type 2O | |||
| autosomal dominant Charcot-Marie-Tooth disease type 2O | |||||
| autosomal dominant axonal Charcot-Marie-Tooth disease type 2O | |||||
| Parent | Is_a | DOID:0050539 | |||
| DOID:0050736 | |||||
| DB_info | Database | OMIM | disease | 614228 | |
| Attribute_of | Gene_by_orthology | WBGene00000962 |
