craniodiaphyseal dysplasia Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
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)
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Genes

8 genes co-occuring with the disease craniodiaphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
SOST sclerostin 1.55424
LRP5 low density lipoprotein receptor-related protein 5 1.20439
LRP6 low density lipoprotein receptor-related protein 6 1.09041
WNT1 wingless-type MMTV integration site family, member 1 0.994017
WNT3A wingless-type MMTV integration site family, member 3A 0.935385
LDLR low density lipoprotein receptor 0.487788
CALCA calcitonin-related polypeptide alpha 0.246448
TGFB1 transforming growth factor, beta 1 0.172291