osteitis fibrosa Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A bone resorption disease that has_material_basis_in hyperparathyroidism which results_in hyperactivity in osteoclasts, deformity, and loss of mass located_in bone. (Human Disease Ontology, DOID_3341)
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Genes

25 genes co-occuring with the disease osteitis fibrosa in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PTH parathyroid hormone 2.47316
ALPPL2 alkaline phosphatase, placental-like 2 1.82278
ALPP alkaline phosphatase, placental 1.82233
ALPL alkaline phosphatase, liver/bone/kidney 1.82142
KNTC1 kinetochore associated 1 1.59028
BGLAP bone gamma-carboxyglutamate (gla) protein 1.26516
CALCA calcitonin-related polypeptide alpha 0.95996
CASR calcium-sensing receptor 0.802795
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor 0.648928
NPSR1 neuropeptide S receptor 1 0.647743
PTHLH parathyroid hormone-like hormone 0.631991
MGAM maltase-glucoamylase 0.584719
PTH1R parathyroid hormone 1 receptor 0.508808
B2M beta-2-microglobulin 0.487788
APEH acylaminoacyl-peptide hydrolase 0.457109
ZNF410 zinc finger protein 410 0.423265
MCM3 minichromosome maintenance complex component 3 0.388909
ACPP acid phosphatase, prostate 0.382223
ALB albumin 0.308118
PDHX pyruvate dehydrogenase complex, component X 0.275445
RHAG Rh-associated glycoprotein 0.221793
EPO erythropoietin 0.213621
GNAS GNAS complex locus 0.202618
HPN hepsin 0.185016
MCM2 minichromosome maintenance complex component 2 0.160574