Cushing's symphalangism Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An autosomal dominant disease that is characterized by ankylosis of the proximal interphalangeal joints, carpal and tarsal bone fusion, and conductive deafness. (Human Disease Ontology, DOID_0050788)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536223
Similar Terms
Downloads & Tools

Genes

2 genes/proteins associated with the disease Cushing's symphalangism from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
NOG noggin 2.88009
GDF5 growth differentiation factor 5 2.88009