Disease #01947 (CMS6 (myasthenic syndrome, congenital, type 6, presynaptic (CMS-6)), OMIM:254210)
Official abbreviation |
CMS6 |
Name |
myasthenic syndrome, congenital, type 6, presynaptic (CMS-6) |
OMIM ID |
254210 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
CHAT |
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.
|