Ovarian hyperstimulation syndrome

Preferred Label : Ovarian hyperstimulation syndrome;

Symbol : OHSS;

CISMeF acronym : OHSS;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Ovarian hyperstimulation syndrome, familial gestational spontaneous;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutations in the follicle-stimulating hormone receptor gene (FSHR, 136435.0008);

Prefixed ID : #608115;

Détails

Origin ID

608115;

UMLS CUI

C0085083;

Currated CISMeF NLP mapping
- Hyperstimulation of ovaries (disorder) [SNOMED CT concept]
- OVARIAN HYPERSTIMULATION [WHO-ART Preferred Term]
- Ovarian hyperstimulation [MedDRA LLT]
- Ovarian hyperstimulation syndrome [PASCAL descriptor]
- Ovarian hyperstimulation syndrome [ICD-11 Subcategory]
- Ovarian hyperstimulation syndrome [MedDRA Preferred Term]
- Ovarian hyperstimulation syndrome [ORDO Disease]
- Ovarian hyperstimulation syndrome (disorder) [SNOMED CT concept]
- ovarian hyperstimulation syndrome [DO Concept]
- ovarian hyperstimulation syndrome [Disease (Nov.)]
- ovarian hyperstimulation syndrome [MeSH Descriptor]
- ovarian hyperstimulation syndrome [MeSH concept]
DO Cross reference
- ovarian hyperstimulation syndrome [DO Concept]
Genes related to phenotype
- Follicle-stimulating hormone receptor [OMIM gene]
HPO term(s)
- Abdominal pain [HPO term]
- Abnormality of the genitourinary system [HPO term]
- Ascites [HPO term]
- Autosomal dominant inheritance [HPO term]
- Nausea [HPO term]
ORDO concept(s)
- Ovarian hyperstimulation syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ovarian hyperstimulation syndrome [MedDRA Preferred Term]
- Ovarian hyperstimulation syndrome [ORDO Disease]
- Ovarian hyperstimulation syndrome (disorder) [SNOMED CT concept]
- ovarian hyperstimulation syndrome [MeSH Descriptor]
- ovarian hyperstimulation syndrome [MeSH concept]
- ovarian hyperstimulation syndrome [DO Concept]
Validated automatic mappings to BTNT
- ovarian hyperstimulation syndrome, familial gestational spontaneous [MeSH concept]

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