craniodiaphyseal dysplasia Gene Set

Dataset	DISEASES Text-mining Gene-Disease Association 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