Disease: Seizures, Sensory ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0751496
Disease: Seizures, Sensory
Seizures, Sensory 		0.300 Biomarker phenotype CTD_human Neurodevelopmental alterations and seizures developed by mouse model of infantile hypophosphatasia are associated with purinergic signalling deregulation. 27466191 2016
CUI: C0751496
Disease: Seizures, Sensory
Seizures, Sensory 		0.300 Therapeutic phenotype CTD_human Neurodevelopmental alterations and seizures developed by mouse model of infantile hypophosphatasia are associated with purinergic signalling deregulation. 27466191 2016
CUI: C0751496
Disease: Seizures, Sensory
Seizures, Sensory 		0.300 Biomarker phenotype CTD_human Mice lacking tissue non-specific alkaline phosphatase die from seizures due to defective metabolism of vitamin B-6. 7550313 1995
CUI: C0751496
Disease: Seizures, Sensory
Seizures, Sensory 		0.300 Therapeutic phenotype CTD_human Mice lacking tissue non-specific alkaline phosphatase die from seizures due to defective metabolism of vitamin B-6. 7550313 1995