Disease #05239 (CMS19 (myasthenic syndrome, congenital, type 19 (CMS-19)), OMIM:616720)
| Official abbreviation |
CMS19 |
| Name |
myasthenic syndrome, congenital, type 19 (CMS-19) |
| OMIM ID |
616720 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
COL13A1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2017-03-19 12:35:33 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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