Link to this page
Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/608115
http://purl.bioontology.org/ontology/OMIM/608115
|
|---|---|
| Preferred Name | OVARIAN HYPERSTIMULATION SYNDROME |
| Synonyms |
OVARIAN HYPERSTIMULATION SYNDROME, FAMILIAL GESTATIONAL SPONTANEOUS
OHSS
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
OVARIAN HYPERSTIMULATION SYNDROME, FAMILIAL GESTATIONAL SPONTANEOUS
OHSS
|
|---|---|
| prefLabel | OVARIAN HYPERSTIMULATION SYNDROME
|
| Gene Symbol |
FSHR
ODG1
|
| Scope Statement | Symptoms occur only during pregnancy (usual onset after 6 weeks gestation) [MISCELLANEOUS]
Caused by mutations in the follicle-stimulating hormone receptor gene (FSHR, 136435.0008) [MOLECULAR BASIS]
Major fluid shifts may occur in severe cases [MISCELLANEOUS]
|
| type | |
| Has manifestation |
See more
See less
|
| tui | T047
|
| Gene Locus | 2p21-p16
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 608115
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui |
C0085083
C3494162
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |