All terms in EPO

Label Id Description
pathway PW_0000001
Abnormal eyelid movement HP_0031785
Abnormal eyelid physiology HP_0031879
hypotonia MP_0004144
Abnormal muscle tone HP_0003808
cystitis DOID_1679
bladder disease DOID_365
carbohydrate metabolic disorder DOID_2978
inherited metabolic disorder DOID_655
Myoclonic status epilepticus HP_0032667
Status epilepticus with prominent motor symptoms HP_0032658
Hyperkinetic status epilepticus HP_0032666
Platyhelminthes NCBITaxon_6157
Eukaryota NCBITaxon_2759
autoimmune disease of the nervous system DOID_438
autoimmune hypersensitivity disease DOID_417
Abnormal circulating protein level HP_0010876
Abnormal circulating metabolite concentration HP_0032180
Abnormality of joint mobility HP_0011729
Abnormality of skeletal physiology HP_0011843