MeSH Browser

MeSH Supplementary: Lyngstadaas syndrome
Unique ID: C537490
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537490
Entry Term(s): Steroid dehydrogenase deficiency dental anomalies
Heading Mapped to: *Tooth, Supernumerary; 3-Hydroxysteroid Dehydrogenases / deficiency; *Steroid Metabolism, Inborn Errors
Frequency: 0
Note: Severe dental aberrations in familial steroid dehydrogenase deficiency
Source: Clin Genet. 49(5):249-54
Date of Entry: 2010/08/25
Revision Date: 2016/07/07

Lyngstadaas syndrome MeSH Supplementary Concept Data 2024