DR info

Clinical trials : 90 / Drugs : 87 - (DrugBank : 30) / Drug target genes : 39 - Drug target pathways : 88

Frontotemporal lobar degeneration and other diseases between which drug repositioning might occur (Sakate and Kimura 2021) . Circle size: Number of drugs, Line breadth: Drug repositionability

ID	Diseases (Sorted by drug repositionability)
127	Frontotemporal lobar degeneration
6	Parkinson disease
2	Amyotrophic lateral sclerosis
13	Multiple sclerosis/Neuromyelitis optica
46	Malignant rheumatoid arthritis
85	Idiopathic interstitial pneumonia
5	Progressive supranuclear palsy
86	Pulmonary arterial hypertension
28	Systemic amyloidosis
8	Huntington disease
256	Muscle glycogenosis
113	Muscular dystrophy
70	Spinal stenosis
3	Spinal muscular atrophy
96	Crohn disease
17	Multiple system atrophy
233	Wolfram syndrome
97	Ulcerative colitis
206	Fragile X syndrome
102	Rubinstein-Taybi syndrome
156	Rett syndrome
58	Hypertrophic cardiomyopathy
34	Neurofibromatosis
215	Tetralogy of Fallot
331	Idiopathic multicentric castleman disease
65	Primary immunodeficiency
168	Ehlers-Danlos syndrome
49	Systemic lupus erythematosus
222	Primary nephrotic syndrome
89	Lymphangioleiomyomatosis
4	Primary lateral sclerosis
90	Retinitis pigmentosa
193	Prader-Willi syndrome
226	Interstitial cystitis with Hunners ulcer
26	HTLV-1-associated myelopathy
38	Stevens-Johnson syndrome
1	Spinal and bulbar muscular atrophy
78	Hypopituitarism
11	Myasthenia gravis
149	Hemiconvulsion hemiplegia epilepsy syndrome
10	Charcot-Marie-Tooth disease
51	Scleroderma
67	Polycystic kidney disease
84	Sarcoidosis
118	Myelomeningocele
203	22q11.2 deletion syndrome
205	Fragile X syndrome related disease
18	Spinocerebellar degeneration
21	Mitochondrial disease
140	Dorabe syndrome
144	Lennox-Gastaut syndrome
36	Epidermolysis bullosa
77	Growth hormone secreting pituitary adenoma
57	Idiopathic dilated cardiomyopathy
169	Menkes disease
170	Occipital horn syndrome
53	Sjogren syndrome
114	Non-dystrophic myotonia syndrome
288	Autoimmune acquired coagulation factor deficiency
299	Cystic fibrosis
107	Juvenile idiopathic arthritis
298	Hereditary pancreatitis
280	Huge arteriovenous malformation with cervicofacial or limb lesion
285	Fanconi anemia
158	Tuberous sclerosis
231	Alpha-1-antitrypsin deficiency
283	Acquired pure red cell aplasia
179	Williams syndrome
60	Aplastic anemia
137	Focal cortical dysplasia
192	Cockayne syndrome
277	Lymphangiomatosis
281	Klippel-Trenaunay-Weber syndrome
52	Mixed connective tissue disease
220	Rapidly progressive glomerulonephritis
30	Distal myopathy