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
|