MeSH Browser

MeSH Supplementary: Hymen, Imperforate
Unique ID: C562397
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562397
Registry Numbers: 0
Heading Mapped to: *Congenital Abnormalities; Hymen / abnormalities
Frequency: 80
Note: A hereditary austosomal recessive condition characterized by an imperforate hymen and AMENORRHEA. HEMATOCOLPOS or HYDROCOLPOS may also be present but internal and external genitalia are usually normal. OMIM: 237100
Date of Entry: 2012/11/05
Revision Date: 2020/02/21

Hymen, Imperforate MeSH Supplementary Concept Data 2025