Leiomyoma of vulva and esophagus

Preferred Label : Leiomyoma of vulva and esophagus;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Leiomyomatosis, esophagogastric and vulvar;

Inheritance : Autosomal dominant;

Prefixed ID : 150700;

Details

Origin ID

150700;

UMLS CUI

C1835488;

Currated CISMeF NLP mapping
- Leiomyoma of vulva and esophagus [MeSH concept]
- leiomyoma of vulva and esophagus [MeSH Supplementary Concept]
False automatic mappings
- Hereditary leiomyomatosis and renal cell cancer [ORDO Disease]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Clitoral hypertrophy [HPO term]
- Esophageal obstruction [HPO term]
ORDO concept(s)
- X-linked Alport syndrome-diffuse leiomyomatosis [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Leiomyoma of vulva and esophagus [MeSH concept]
- leiomyoma of vulva and esophagus [MeSH Supplementary Concept]

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