Disease #05890 (ZLS3 (Zimmermann-Laband syndrome, type 3 (ZLS3)), OMIM:618658)
| Official abbreviation |
ZLS3 |
| Name |
Zimmermann-Laband syndrome, type 3 (ZLS3) |
| OMIM ID |
618658 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
KCNN3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-01-12 16:48:31 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|