Fremanezumab

DrugBank ID: DB14041


Summary

Metric Value
Total Predictions 50
KG+DL (Dual Validated) 1
DL Only 49
KG Only 0

Predictions

Indication Score Source
migraine with brainstem aura 0.9994 DL
migraine disorder 0.9994 KG+DL
migraine with or without aura, susceptibility to 0.9934 DL
atrophoderma vermiculata 0.9904 DL
ulerythema ophryogenesis 0.9864 DL
heparin cofactor 2 deficiency 0.9688 DL
antithrombin deficiency type 2 0.9637 DL
factor 5 excess with spontaneous thrombosis 0.9625 DL
thrombophilia 0.9431 DL
amenorrhea (disease) 0.9274 DL
sciatic neuropathy 0.9032 DL
hemorrhagic disease of newborn 0.8075 DL
severe nonproliferative diabetic retinopathy 0.6597 DL
hyperemesis gravidarum (disease) 0.6424 DL
hyperparathyroidism, primary, caused by water clear cell hyperplasia 0.6019 DL
omphalocele (disease) 0.5979 DL
sudden arrhythmia death syndrome 0.5933 DL
cauda equina syndrome 0.5898 DL
prekallikrein deficiency 0.5892 DL
Coronavinae infectious disease 0.5876 DL
tibial adamantinoma 0.5843 DL
non-specific granulomatous orchitis 0.5820 DL
cholangiocarcinoma, susceptibility to 0.5817 DL
Taylor syndrome 0.5803 DL
adhesions of uterus 0.5803 DL
chronic subinvolution of uterus 0.5803 DL
female infertility of uterine origin 0.5803 DL
uterine inversion 0.5803 DL
amelia of upper limb 0.5780 DL
male infertility due to sperm disorder 0.5753 DL
polydactyly of an index finger, unilateral 0.5744 DL
Marin-Amat syndrome 0.5740 DL
inverse Marcus-Gunn phenomenon 0.5740 DL
split foot, bilateral 0.5677 DL
split foot, unilateral 0.5677 DL
Polymerase proofreading-related adenomatous polyposis 0.5670 DL
alacrima, congenital 0.5663 DL
mitral valve prolapse, myxomatous 0.5655 DL
writing disorder 0.5650 DL
PDA1 0.5644 DL
aphasia 0.5638 DL
mixed receptive-expressive language disorder 0.5638 DL
T-cell immunodeficiency 0.5627 DL
congenital cystic eye multiple ocular and intracranial anomalies 0.5618 DL
ossifying fibroma (disease) 0.5605 DL
terminal transverse defects of arm 0.5596 DL
hypercarotenemia and vitamin A deficiency, autosomal recessive 0.5592 DL
trichostrongylosis 0.5591 DL
odontochondrodysplasia 2 with hearing loss and diabetes 0.5580 DL
Celosomia 0.5574 DL


Disclaimer
Predictions are for research purposes only and do not constitute medical advice.

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