Disease #04311 (CMS-7 (myasthenic syndrome, congenital, type 7, presynaptic (CMS-7)), OMIM:616040)
Official abbreviation |
CMS-7 |
Name |
myasthenic syndrome, congenital, type 7, presynaptic (CMS-7) |
OMIM ID |
616040 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
SYT2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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