Charcot-Marie-Tooth disease type 1C
Information
- Disease name
- Charcot-Marie-Tooth disease type 1C
- Disease ID
- DOID:0110151
- Description
- "A Charcot-Marie-Tooth disease type 1 that has_material_basis_in heterozygous mutation in the LITAF gene on chromosome 16p13." [url:https\://www.ncbi.nlm.nih.gov/pubmed/12525712]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT05902351 | Recruiting | Natural History Study for Charcot Marie Tooth Disease | November 1, 2013 | December 31, 2029 |
- Disase is a (Disease Ontology)
- DOID:0050538
- Cross Reference ID (Disease Ontology)
- ICD10CM:G60.0
- Cross Reference ID (Disease Ontology)
- MESH:C537984
- Cross Reference ID (Disease Ontology)
- MIM:601098
- Cross Reference ID (Disease Ontology)
- ORDO:101083
- Exact Synonym (Disease Ontology)
- Charcot-Marie-Tooth neuropathy type 1C
- Exact Synonym (Disease Ontology)
- CMT slow nerve conduction type C
- Exact Synonym (Disease Ontology)
- CMT1C
- Exact Synonym (Disease Ontology)
- HMSN IC
- Exact Synonym (Disease Ontology)
- HMSN1C
- Exact Synonym (Disease Ontology)
- neuropathy hereditary motor and sensory type 1C