Disease #05492 (SWILS (Saul-Wilson syndrome (SWILS)), OMIM:618150)
| Official abbreviation |
SWILS |
| Name |
Saul-Wilson syndrome (SWILS) |
| OMIM ID |
618150 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
14 |
| Phenotype entries for this disease |
14 |
| Associated with 1 gene |
COG4 |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2018-10-28 22:51:27 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|