idiopathic juvenile osteoporosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An osteoporosis with no known cause that is characterized by pain in the back and extremities, walking difficulties, multiple fractures, and radiological evidence of osteoporosis. (Human Disease Ontology, DOID_12559)
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10 genes co-occuring with the disease idiopathic juvenile osteoporosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
LRP5 low density lipoprotein receptor-related protein 5 1.62873
COL1A2 collagen, type I, alpha 2 1.15112
PTH parathyroid hormone 0.986428
CALCA calcitonin-related polypeptide alpha 0.848716
NIPBL Nipped-B homolog (Drosophila) 0.837656
ALPPL2 alkaline phosphatase, placental-like 2 0.506507
ALPP alkaline phosphatase, placental 0.506123
ALPL alkaline phosphatase, liver/bone/kidney 0.505739
COL1A1 collagen, type I, alpha 1 0.430768
RUNX2 runt-related transcription factor 2 0.424014