Disease #02362 (CMT4D (Charcot-Marie-Tooth disease, type 4D (CMT-4D)), OMIM:601455)
| Official abbreviation |
CMT4D |
| Name |
Charcot-Marie-Tooth disease, type 4D (CMT-4D) |
| OMIM ID |
601455 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
NDRG1 |
| 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
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|