Carbetocin

DrugBank ID: DB01282

Summary

Metric	Value
Total Predictions	51
KG+DL (Dual Validated)	1
DL Only	49
KG Only	1

Predictions

Indication	Score	Source
isotretinoin-like syndrome	0.9915	DL
Goodman syndrome	0.9906	DL
Prader-Willi syndrome due to paternal deletion of 15q11q13	0.9899	DL
Brachymorphism-onychodysplasia-dysphalangism syndrome	0.9898	DL
Mietens syndrome	0.9896	DL
hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome	0.9895	DL
lethal faciocardiomelic dysplasia	0.9895	DL
symptomatic form of Coffin-Lowry syndrome in female carriers	0.9894	DL
hypoglossia-hypodactyly syndrome	0.9893	DL
partial deletion of the long arm of chromosome 15	0.9893	DL
chromosome 16p13.3 deletion syndrome	0.9891	DL
short stature-wormian bones-dextrocardia syndrome	0.9891	DL
moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome	0.9890	DL
2q24 microdeletion syndrome	0.9888	DL
syndrome caused by partial chromosomal duplication	0.9886	DL
4q25 proximal deletion syndrome	0.9882	DL
Robinow-like syndrome	0.9881	DL
arachnodactyly-intellectual disability-dysmorphism syndrome	0.9881	DL
multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome	0.9880	DL
metopic ridging-ptosis-facial dysmorphism syndrome	0.9880	DL
chromosome 1, uniparental disomy 1q12 q21	0.9879	DL
chromosome 12p deletion	0.9879	DL
chromosome 13p duplication	0.9879	DL
chromosome 13q trisomy	0.9879	DL
chromosome 13q-mosaicism	0.9879	DL
chromosome 16 trisomy	0.9879	DL
chromosome 18 mosaic monosomy	0.9879	DL
chromosome 1q deletion	0.9879	DL
chromosome 20 trisomy	0.9879	DL
chromosome 22, monosome mosaic	0.9879	DL
chromosome 22q deletion	0.9879	DL
chromosome inversion	0.9879	DL
gonosome anomaly	0.9878	DL
monosomy	0.9877	DL
uniparental disomy of maternal origin	0.9876	DL
autosomal anomaly	0.9874	DL
chromosome 17 abnormality	0.9870	DL
oculotrichoanal syndrome	0.9864	DL
chromosome 1p32-p31 deletion syndrome	0.9831	DL
Prader-Willi syndrome	0.9803	KG+DL
monosomy X	0.9496	DL
Turner syndrome	0.8919	DL
dysmorphism-conductive hearing loss-heart defect syndrome	0.8794	DL
dyschondrosteosis-nephritis syndrome	0.8762	DL
retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome	0.8728	DL
thyrocerebrorenal syndrome	0.8722	DL
46,XX disorder of sex development-anorectal anomalies syndrome	0.8575	DL
Mayer-Rokitansky-Kuster-Hauser syndrome	0.8546	DL
torticollis-keloids-cryptorchidism-renal dysplasia syndrome	0.8543	DL
lower limb deficiency-hypospadias syndrome	0.8524	DL

Showing top 50 of 51 predictions.

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