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 |
|