Cytoscape Web
Click node...

Atypical dentin dysplasia due to SMOC2 deficiency
1 OMIM reference -
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
Nestor-Guillermo progeria syndrome
Synonym(s):
- Dentin dysplasia type 1 with microdontia and shape anomalies
Classification (Orphanet):
- Rare genetic disease
- Rare odontologic disease
Classification (ICD10):
- Diseases of the digestive system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SMOC2 Q9H3U7607223
No signs/symptoms info available.