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Lyngstadaas syndrome MeSH Supplementary Concept Data 2022


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
Registry Number
0
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 Preferred
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