Disease #01247 (CMT1A (Charcot-Marie-Tooth disease, type IA (CMT1A)), OMIM:118220)
| Official abbreviation |
CMT1A |
| Name |
Charcot-Marie-Tooth disease, type IA (CMT1A) |
| OMIM ID |
118220 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PMP22 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-06-30 17:23:15 +02:00 (CEST) |
Individuals
|