hasPhenotype

185 triples
GPTKB property

Alternative names (5)
associated phenotype associatedWithPhenotype has phenotype phenotype phenotypes

Random 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

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