fibrogenesis imperfecta ossium Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A syndrome that involves abnormality of collagen synthesis in lamellar bones, with manifestations limited to the skeleton. The initial symptom is frequently spontaneous fractures. (Human Disease Ontology, DOID_0080040)
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Genes

3 genes co-occuring with the disease fibrogenesis imperfecta ossium in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
ALPPL2 alkaline phosphatase, placental-like 2 0.812232
ALPP alkaline phosphatase, placental 0.811411
ALPL alkaline phosphatase, liver/bone/kidney 0.811001