Disease #02698 (CMT1F (Charcot-Marie-Tooth disease, type IF (CMT-1F)), OMIM:607734)
Official abbreviation |
CMT1F |
Name |
Charcot-Marie-Tooth disease, type IF (CMT-1F) |
OMIM ID |
607734 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Autosomal recessive |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
NEFL |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|