Disease #02737 (OHSS (ovarian hyperstimulation syndrome), OMIM:608115)
Official abbreviation |
OHSS |
Name |
ovarian hyperstimulation syndrome |
OMIM ID |
608115 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
FSHR |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2023-02-08 10:20:02 +01:00 (CET) |
Individuals
|