Disease #05223 (CMS20 (myasthenic syndrome, congenital, type 20, presynaptic (CMS-20)), OMIM:617143)
Official abbreviation |
CMS20 |
Name |
myasthenic syndrome, congenital, type 20, presynaptic (CMS-20) |
OMIM ID |
617143 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
6 |
Phenotype entries for this disease |
6 |
Associated with 1 gene |
SLC5A7 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2017-02-10 16:34:12 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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