| Human Disease |
Term: Hereditary Motor and Sensory Neuropathy, Type IIC; HMSN2C
OMIM ID: 606071
|
| Synonyms |
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2C; CMT2C; Charcot-Marie-Tooth Neuropathy, Type 2C; HMSN IIC |
| Associated Genes |
Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.
Mouse Gene |
Human Gene |
|
Characteristics of this human disease are associated with mutations in... |
| |
|
|
|
|
 ...the human gene.
MGI data currently do not associate this disease with mutations in the orthologous mouse gene. |
| |
|
|
|
Analysis Tools