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
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