|Name||split hand/foot malformation (ectrodactyly) type 5|
|NCBI Gene ID||171157|
|Expression in Tissues and Cell Lines||
SHFM5 has 3 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 2 datasets.
Click the + buttons to view associations for SHFM5 from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with SHFM5 gene/protein from the curated CTD Gene-Disease Associations dataset.|
|OMIM Gene-Disease Associations||phenotypes associated with SHFM5 gene from the curated OMIM Gene-Disease Associations dataset.|