Lapatinib

Basic Information

Item Value
DrugBank ID DB01259
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 62

Predicted Indications (TxGNN)

The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.

# Indication Source
1 dermatofibrosarcoma protuberans KG + DL
2 fibroblastic neoplasm KG + DL
3 conventional fibrosarcoma KG + DL
4 kidney fibrosarcoma KG + DL
5 cysticercosis KG + DL
6 heart fibrosarcoma KG + DL
7 low grade fibromyxoid sarcoma KG + DL
8 Plasmodium falciparum malaria KG + DL
9 coenurosis KG + DL
10 lymphangiomyoma KG + DL
11 benign PEComa KG + DL
12 uterine corpus perivascular epithelioid cell tumor KG + DL
13 autosomal recessive familial Mediterranean fever KG + DL
14 liver fibrosarcoma KG + DL
15 cutaneous undifferentiated pleomorphic sarcoma KG + DL
16 central nervous system fibrosarcoma KG + DL
17 normal breast-like subtype of breast carcinoma KG + DL
18 progesterone-receptor positive breast cancer KG + DL
19 progesterone-receptor negative breast cancer KG + DL
20 breast tumor luminal A or B KG + DL
21 cutaneous leiomyosarcoma (disease) KG + DL
22 Marfan syndrome KG + DL
23 gallbladder leiomyosarcoma KG + DL
24 situs inversus KG + DL
25 lymphangioleiomyomatosis KG + DL
26 diaphragmatic or abdominal wall malformation KG + DL
27 paralytic facial malformation KG + DL
28 hypoglossia/aglossia KG + DL
29 external auditory canal aplasia/hypoplasia KG + DL
30 congenital limb malformation KG + DL
31 digestive tract malformation KG + DL
32 breast fibrosarcoma KG + DL
33 bone fibrosarcoma KG + DL
34 malformation syndrome with hamartosis KG + DL
35 facial cleft KG + DL
36 cutis laxa - Marfanoid syndrome KG + DL
37 tuberous sclerosis KG + DL
38 lung PEComa KG + DL
39 pseudodiastrophic dysplasia KG + DL
40 synovium cancer KG + DL
41 heart position anomaly KG + DL
42 cleft lip with or without cleft palate KG + DL
43 cranial malformation KG + DL
44 laterality defects, autosomal dominant KG + DL
45 obsolete Marfan syndrome type 2 KG + DL
46 familial Mediterranean fever, autosomal dominant KG + DL
47 tenosynovial giant cell tumor KG + DL
48 situs ambiguus KG + DL
49 fusariosis KG + DL
50 familial caudal dysgenesis KG + DL

(Showing top 50 of 62 predictions)

Disclaimer

These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.


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