Alternative names (5)
associated phenotype • associatedWithPhenotype • has phenotype • phenotype • phenotypesRandom triples
| Subject | Object |
|---|---|
| gptkb:Nr1h3 | impaired lipid homeostasis |
| gptkb:FBgn0000575 | white eye color |
| gptkb:Spontaneously_Hypertensive_Rat | renal injury |
| gptkb:Nf1_knockout_mouse | abnormal neural development |
| gptkb:BALB/cJ | high IgE response |
| gptkb:SOD1-G93A_transgenic_mouse | paralysis |
| gptkb:chr2q37.3 | gptkb:intellectual_disability |
| gptkb:Immunodeficiency_18 | impaired B cell function |
| gptkb:Duffy_antigen | Fy(a+b-) |
| gptkb:OMIM:160790 | elevated sweat chloride |
| gptkb:SOD1-G93A_mouse | progressive motor neuron degeneration |
| gptkb:Silver-Russell_syndrome_(mouse_model) | asymmetry |
| gptkb:Silver-Russell_syndrome_(mouse_model) | craniofacial abnormalities |
| gptkb:OMIM:607709 | fasciculations |
| gptkb:Temple-Baraitser_syndrome | delayed development |
| gptkb:Spontaneously_Hypertensive_Rat | increased risk of stroke |
| gptkb:C._elegans_unc-51 | uncoordinated movement |
| gptkb:BALB/cJ | albino |
| gptkb:Silver-Russell_syndrome_(mouse_model) | growth retardation |
| gptkb:BALB/cByJ | susceptible to plasmacytomas |