Alternative names (5)
associated phenotype • associatedWithPhenotype • has phenotype • phenotype • phenotypesRandom triples
| Subject | Object |
|---|---|
| gptkb:SHFM4 | limb malformation |
| gptkb:SOD1-G93A_mouse | progressive motor neuron degeneration |
| gptkb:MGI:96433 | increased tumor incidence |
| gptkb:BALB/cJ | high IgE response |
| gptkb:YDR179C | defective transcriptional regulation |
| gptkb:YGL195W | petite negative |
| gptkb:OMIM_109700 | elevated sweat chloride |
| gptkb:Temple-Baraitser_syndrome | broad nasal bridge |
| gptkb:Fanconi_anemia,_complementation_group_M | congenital abnormalities |
| gptkb:OMIM:607709 | progressive muscle weakness |
| gptkb:CYP2D6 | ultrarapid metabolizer |
| gptkb:MIM_109700 | chronic respiratory infections |
| gptkb:FBgn0000575 | white eye color |
| gptkb:AGTR2_gene | intellectual disability (in some mutations) |
| gptkb:Duffy_antigen | Fy(a-b-) |
| gptkb:Nr1h3 | impaired lipid homeostasis |
| gptkb:LCA10 | photophobia |
| gptkb:Oca2_(mouse) | pink eyes |
| gptkb:SOD1-G93A_transgenic_mouse | reduced lifespan |
| gptkb:FBgn0000577 | viability |