Dwarfism Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A severe degree of short stature, more than -4 SD from the mean corrected for age and sex. (Human Phenotype Ontology, HP_0003510)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D004392
Similar Terms
Downloads & Tools

Genes

5 genes/proteins associated with the disease Dwarfism from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
WNT4 wingless-type MMTV integration site family, member 4 2.88009
TG thyroglobulin 2.88009
PLK4 polo-like kinase 4 2.88009
HAPLN1 hyaluronan and proteoglycan link protein 1 2.88009
ORC1 origin recognition complex, subunit 1 2.88009