Disease: Other emphysema ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0029607
Disease: Other emphysema
Other emphysema 		0.200 Biomarker phenotype MGD Defective release of α granule and lysosome contents from platelets in mouse Hermansky-Pudlak syndrome models. 25477496 2015
CUI: C0029607
Disease: Other emphysema
Other emphysema 		0.200 Biomarker phenotype MGD Iris phenotypes and pigment dispersion caused by genes influencing pigmentation. 18715234 2008
CUI: C0029607
Disease: Other emphysema
Other emphysema 		0.200 Biomarker phenotype MGD Gravity receptor function in mice with graded otoconial deficiencies. 15109702 2004
CUI: C0029607
Disease: Other emphysema
Other emphysema 		0.200 Biomarker phenotype MGD Biogenesis of lysosome-related organelles complex 3 (BLOC-3): a complex containing the Hermansky-Pudlak syndrome (HPS) proteins HPS1 and HPS4. 12847290 2003
CUI: C0029607
Disease: Other emphysema
Other emphysema 		0.200 Biomarker phenotype MGD Pulmonary pathologies in pallid mice result from nonhematopoietic defects. 12009785 2002
CUI: C0029607
Disease: Other emphysema
Other emphysema 		0.200 Biomarker phenotype MGD Melanosome morphologies in murine models of hermansky-pudlak syndrome reflect blocks in organelle development. 12445206 2002
CUI: C0029607
Disease: Other emphysema
Other emphysema 		0.200 Biomarker phenotype MGD Survival and lung pathology of mouse models of Hermansky-Pudlak syndrome and Chediak-Higashi syndrome. 10193444 1999
CUI: C0029607
Disease: Other emphysema
Other emphysema 		0.200 Biomarker phenotype MGD The pallid mouse. A model of genetic alpha 1-antitrypsin deficiency. 8441253 1993
CUI: C0029607
Disease: Other emphysema
Other emphysema 		0.200 Biomarker phenotype MGD Platelet storage pool deficiency in mouse pigment mutations associated with seven distinct genetic loci. 6696991 1984
CUI: C0029607
Disease: Other emphysema
Other emphysema 		0.200 Biomarker phenotype MGD Pigment mutations in the mouse which also affect lysosomal functions lead to suppressed natural killer cell activity. 7089489 1982
CUI: C0029607
Disease: Other emphysema
Other emphysema 		0.200 Biomarker phenotype MGD Lysosomal dysfunctions associated with mutations at mouse pigment genes. 115747 1979
CUI: C0029607
Disease: Other emphysema
Other emphysema 		0.200 Biomarker phenotype MGD Prevention of congenital otolith defect in pallid mutant mice by manganese supplementation. 5559839 1971