hasPhenotype

URI: https://gptkb.org/prop/hasPhenotype

185 triples

GPTKB property

associated phenotype • associatedWithPhenotype • has phenotype • phenotype • phenotypes

Subject	Object
gptkb:OMIM_109700	elevated sweat chloride
gptkb:SOD1-G93A_mouse	paralysis
gptkb:rd8_mouse	photoreceptor degeneration
gptkb:SOD1-G93A_transgenic_mouse	motor neuron degeneration
gptkb:Spontaneously_Hypertensive_Rat	hyperactivity
gptkb:splashed_white	white legs
gptkb:chr2q37.3	gptkb:intellectual_disability
gptkb:Fanconi_anemia,_complementation_group_M	congenital abnormalities
gptkb:SOD1-G93A_transgenic_mouse	paralysis
gptkb:OMIM:607709	dysphagia
gptkb:FUS_transgenic_mouse	neurodegeneration
gptkb:FBgn0000095	white eyes
gptkb:Neurotrophic_tyrosine_kinase_receptor_type_1_(mouse)	pain perception
gptkb:YNL005C	affects mRNA stability
gptkb:AK_mouse_strain_(thymoma)	susceptible to spontaneous thymic lymphoma
gptkb:OMIM:160790	chronic pulmonary disease
gptkb:Fanconi_anemia,_complementation_group_D2	increased risk of acute myeloid leukemia
gptkb:Silver-Russell_syndrome_(mouse_model)	growth retardation
gptkb:Spontaneously_Hypertensive_Rat	renal injury
gptkb:Temple-Baraitser_syndrome	thick vermilion of lips