congenital intrinsic factor deficiency Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A vitamin B12 deficiency that is characterized by megaloblastic anemia due to the absence of gastric intrinsic factor which results in abnormal vitamin B12 absorption. (Human Disease Ontology, DOID_0050734)
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Genes

2 genes co-occuring with the disease congenital intrinsic factor deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
GIF gastric intrinsic factor (vitamin B synthesis) 1.81645
F3 coagulation factor III (thromboplastin, tissue factor) 0.406051