RGD DISEASE ONTOLOGY - ANNOTATIONS
RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term: ovarian hyperstimulation syndrome
Accession: DOID:5425
browse the term
Definition: An ovarian disease that is characterized by cystic enlargement of the ovaries and a fluid shift from the intravascular to the third space and has_symptom abdominal pain, has_symptom nausea and has_symptom vomiting. This disease is an iatrogenic complication of assisted reproduction technology. (DO)
Synonyms: exact_synonym: OHSS; ovarian hyperstimulation syndrome, familial gestational spontaneous; ovarian hyperstimulation syndromes; ovarian response to FSH stimulation; secondary Meig's syndrome
xref: MESH:D016471 ; MIM:276400 ; MIM:608115 ; MONDO:0011972
For additional species annotation, visit the
Alliance of Genome Resources .
G
Drd2
dopamine receptor D2
treatment
IDA
RGD
PMID:25217874
RGD:13506956
NCBI chr 8:49,708,927...49,772,876
Ensembl chr 8:49,708,927...49,772,875
G
F3
coagulation factor III, tissue factor
severity
ISO
protein:increased expression:plasma
RGD
PMID:12695751
RGD:11340210
NCBI chr 2:209,827,061...209,838,666
Ensembl chr 2:209,826,959...209,838,668
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Fshr
follicle stimulating hormone receptor
ISO
DNA:point mutation:exon:D567N ClinVar Annotator: match by term: Ovarian hyperstimulation syndrome CTD Direct Evidence: marker/mechanism
ClinVar CTD OMIM RGD
PMID:8894317 PMID:9402264 PMID:9769327 PMID:10022448 PMID:11213123 PMID:12930927 PMID:12930928 PMID:15080154 PMID:15249125 PMID:15579795 PMID:15886248 PMID:16084888 PMID:16278261 PMID:16864747 PMID:17721928 PMID:17826728 PMID:18159088 PMID:19400992 PMID:21752882 PMID:22401810 PMID:22414334 PMID:23419799 PMID:25741868 PMID:28492532 PMID:12930928 More...
RGD:1601236
NCBI chr 6:5,198,825...5,406,785
Ensembl chr 6:5,198,825...5,406,785
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Il6
interleukin 6
ISO
protein:increased expression:serum, ascites (human)
RGD
PMID:9322101
RGD:11062135
NCBI chr 4:5,214,602...5,219,178
Ensembl chr 4:5,213,394...5,219,178
G
Kdr
kinase insert domain receptor
treatment
IEP
RGD
PMID:25151950
RGD:126925217
NCBI chr14:32,217,871...32,261,018
Ensembl chr14:32,217,871...32,261,018
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Nr1h3
nuclear receptor subfamily 1, group H, member 3
ISS
OMIM:608115
MouseDO
NCBI chr 3:77,158,808...77,168,907
Ensembl chr 3:77,158,808...77,168,722
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Serpinf1
serpin family F member 1
treatment
ISO
human protein in a mouse model
RGD
PMID:23295464
RGD:8635395
NCBI chr10:60,250,198...60,262,593
Ensembl chr10:60,249,708...60,262,646
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Tfpi
tissue factor pathway inhibitor
severity
ISO
protein:decreased expression:plasma
RGD
PMID:12695751
RGD:11340210
NCBI chr 3:69,533,156...69,582,547
Ensembl chr 3:69,533,156...69,576,880
G
Vegfa
vascular endothelial growth factor A
treatment
IMP
RGD
PMID:25151950
RGD:126925217
NCBI chr 9:14,955,300...14,970,641
Ensembl chr 9:14,955,300...14,970,641
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