Ovarian fibromata

Preferred Label : Ovarian fibromata;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 166970;

Details

Origin ID

166970;

UMLS CUI

C0149951;

Currated CISMeF NLP mapping
- Fibroma of ovary (disorder) [SNOMED CT concept]
- Ovarian Fibroma [NCIt concept]
- Ovarian fibroma [HPO term]
- Ovarian fibroma [MedDRA Preferred Term]
- Ovarian fibroma [ORDO Disease]
- ovarian fibromata [MeSH concept]
- ovarian fibromata [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Ovarian fibroma [HPO term]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Fibroma of ovary (disorder) [SNOMED CT concept]
- Ovarian Fibroma [NCIt concept]
- Ovarian fibroma [MedDRA Preferred Term]
- Ovarian fibroma [HPO term]
- Ovarian fibroma [ORDO Disease]
- ovarian fibromata [MeSH Supplementary Concept]
- ovarian fibromata [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients