|Name||Otodental dysplasia chromosome deletion syndrome|
|NCBI Gene ID||100885788|
|Expression in Tissues and Cell Lines||
OTDD has 1 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 1 datasets.
Click the + buttons to view associations for OTDD from the datasets below.
If available, associations are ranked by standardized value
|OMIM Gene-Disease Associations||phenotypes associated with OTDD gene from the curated OMIM Gene-Disease Associations dataset.|