Craniodiaphyseal Dysplasia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An osteosclerosis that results_in increased calcium concentration located_in skull which decreases the size of cranium foramina and cervical spinal canal. (Human Disease Ontology, DOID_0080032)
External Link https://www.disgenet.org/browser/0/1/0/C0410539
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Genes

7 genes associated with the disease Craniodiaphyseal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CDA cytidine deaminase
CDKL5 cyclin-dependent kinase-like 5
CLIP1 CAP-GLY domain containing linker protein 1
CXCL8 chemokine (C-X-C motif) ligand 8
GRIA2 glutamate receptor, ionotropic, AMPA 2
NPPA natriuretic peptide A
SOST sclerostin