Disease #04318 (CMS4A (myasthenic syndrome, congenital, type 4A, slow-channel (CMS-4A)), OMIM:605809)
Official abbreviation |
CMS4A |
Name |
myasthenic syndrome, congenital, type 4A, slow-channel (CMS-4A) |
OMIM ID |
605809 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Autosomal recessive |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
CHRNE |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-08-28 21:27:12 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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