| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A bone remodeling disease that has_material_basis_in a vitamin D deficiency in children which results_in softening and deformity located_in bone. (Experimental Factor Ontology, EFO_0005583) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D012279 |
| Similar Terms | |
| Downloads & Tools |
6 genes/proteins associated with the disease Rickets from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| CYP27B1 | cytochrome P450, family 27, subfamily B, polypeptide 1 | 2.88009 |
| VDR | vitamin D (1,25- dihydroxyvitamin D3) receptor | 2.88009 |
| PTH | parathyroid hormone | 2.88009 |
| PTH1R | parathyroid hormone 1 receptor | 2.88009 |
| CYP24A1 | cytochrome P450, family 24, subfamily A, polypeptide 1 | 1.44544 |
| FGF23 | fibroblast growth factor 23 | 1.21727 |
