MeSH Browser

MeSH Supplementary: Single upper central incisor
Unique ID: C537342
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537342
Entry Term(s): Fused incisors; Incisors, Fused; SMMCI Solitary median maxillary central incisor; SMMCI Syndrome; Single central maxillary incisor; Solitary median maxillary central incisor; Solitary median maxillary central incisor syndrome
Registry Numbers: 0
Heading Mapped to: *Anodontia; Incisor / abnormalities
Frequency: 33
Note: A hereditary autosomal dominant condition characterized primarily by single (unpaired) deciduous and permanent maxillary central incisors and short stature. Growth hormone deficiencies may also be present. Mutations in the SHH gene have been identified. OMIM: 147250
Date of Entry: 2010/08/25
Revision Date: 2019/06/20

Single upper central incisor MeSH Supplementary Concept Data 2025