Disease #05176 (CMT2A2A (Charcot-Marie-Tooth disease, type 2A2A (CMT2A2A)), OMIM:609260)
| Official abbreviation |
CMT2A2A |
| Name |
Charcot-Marie-Tooth disease, type 2A2A (CMT2A2A) |
| OMIM ID |
609260 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
59 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
MFN2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2016-07-27 21:11:22 +02:00 (CEST) |
| Date last edited |
2021-01-12 13:04:56 +01:00 (CET) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|