MeSH Browser

MeSH Supplementary: Bifid nose
Unique ID: C535441
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535441
Entry Term(s): Bifid Nose, Autosomal Dominant; Bifid Nose, Autosomal Recessive; Median fissure of nose; Nose, median cleft of
Registry Numbers: 0
Heading Mapped to: Nose / abnormalities; *Nose Diseases
Frequency: 26
Note: Hereditary autosomal dominant (OMIM: 109740) or recessive (OMIM: 210400) nose abnormalities where the nostrils are separated by a cleft or fissure. Individuals with autosomal dominant cases may also present with SCOLIOSIS; BLEPHAROPTOSIS; and CRYPTORCHIDISM.
Date of Entry: 2010/08/25
Revision Date: 2015/09/25

Bifid nose MeSH Supplementary Concept Data 2025