Disease #02339 (CMT1C (Charcot-Marie-Tooth disease, type IC (CMT-1C)), OMIM:601098)
Official abbreviation |
CMT1C |
Name |
Charcot-Marie-Tooth disease, type IC (CMT-1C) |
OMIM ID |
601098 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
9 |
Phenotype entries for this disease |
9 |
Associated with 1 gene |
LITAF |
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
|