Alternative names (5)
associated phenotype • associatedWithPhenotype • has phenotype • phenotype • phenotypesRandom triples
| Subject | Object |
|---|---|
| gptkb:OMIM:160790 | male infertility |
| gptkb:RhD | Rh negative |
| gptkb:Spontaneously_Hypertensive_Rat | proteinuria |
| gptkb:FBgn0003461 | segment polarity defect |
| gptkb:Nr1h3 | altered cholesterol metabolism |
| gptkb:Fanconi_anemia,_complementation_group_D2 | skin pigmentation abnormalities |
| gptkb:MGI:88057 | abnormal cell cycle |
| gptkb:OMIM:607709 | dysphagia |
| gptkb:Fanconi_anemia,_complementation_group_D2 | short stature |
| gptkb:BALB/cJ | susceptible to developing plasmacytomas |
| gptkb:CYP2D6 | extensive metabolizer |
| gptkb:WBGene00003013 | paralyzed |
| gptkb:AGTR2_gene | X-linked mental retardation |
| gptkb:FUS_transgenic_mouse | motor neuron degeneration |
| gptkb:splashed_white | blue eyes |
| gptkb:OMIM:160790 | exocrine pancreatic insufficiency |
| gptkb:Fanconi_anemia,_complementation_group_C | skin pigmentation abnormalities |
| gptkb:AK_mouse_strain_(thymoma) | susceptible to spontaneous thymic lymphoma |
| gptkb:OMIM_109700 | exocrine pancreatic insufficiency |
| gptkb:Nipped-B_(Drosophila) | wing development defects |