Disease: HERMANSKY-PUDLAK SYNDROME 2 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1842362
Disease: HERMANSKY-PUDLAK SYNDROME 2
HERMANSKY-PUDLAK SYNDROME 2 		0.200 Biomarker disease MGD Gravity receptor function in mice with graded otoconial deficiencies. 15109702 2004
CUI: C1842362
Disease: HERMANSKY-PUDLAK SYNDROME 2
HERMANSKY-PUDLAK SYNDROME 2 		0.200 Biomarker disease MGD Mouse models of Hermansky Pudlak syndrome: a review. 9585243 1998
CUI: C1842362
Disease: HERMANSKY-PUDLAK SYNDROME 2
HERMANSKY-PUDLAK SYNDROME 2 		0.200 Biomarker disease MGD Mutation in AP-3 delta in the mocha mouse links endosomal transport to storage deficiency in platelets, melanosomes, and synaptic vesicles. 9697856 1998
CUI: C1842362
Disease: HERMANSKY-PUDLAK SYNDROME 2
HERMANSKY-PUDLAK SYNDROME 2 		0.200 Biomarker disease MGD Mocha, a new coat color and behavior mutation on chromosome 10 of the mouse. 4448900 1975