DR info

Clinical trials : 126 / Drugs : 135 - (DrugBank : 42) / Drug target genes : 46 - Drug target pathways : 162

Hypertrophic cardiomyopathy 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)
58	Hypertrophic cardiomyopathy
13	Multiple sclerosis/Neuromyelitis optica
46	Malignant rheumatoid arthritis
6	Parkinson disease
51	Scleroderma
86	Pulmonary arterial hypertension
96	Crohn disease
97	Ulcerative colitis
113	Muscular dystrophy
222	Primary nephrotic syndrome
2	Amyotrophic lateral sclerosis
226	Interstitial cystitis with Hunners ulcer
85	Idiopathic interstitial pneumonia
28	Systemic amyloidosis
38	Stevens-Johnson syndrome
107	Juvenile idiopathic arthritis
34	Neurofibromatosis
50	Dermatomyositis
164	Oculocutaneous albinism
70	Spinal stenosis
84	Sarcoidosis
65	Primary immunodeficiency
299	Cystic fibrosis
151	Rasmussen encephalitis
298	Hereditary pancreatitis
67	Polycystic kidney disease
127	Frontotemporal lobar degeneration
168	Ehlers-Danlos syndrome
228	Bronchiolitis obliterans
167	Marfan syndrome
90	Retinitis pigmentosa
302	Leber hereditary optic neuropathy
256	Muscle glycogenosis
11	Myasthenia gravis
36	Epidermolysis bullosa
57	Idiopathic dilated cardiomyopathy
53	Sjogren syndrome
269	Pyogenic arthritis
224	Purpura nephritis
227	Osler disease
193	Prader-Willi syndrome
39	Toxic epidermal necrolysis
66	IgA nephropathy
158	Tuberous sclerosis
26	HTLV-1-associated myelopathy
272	Fibrodysplasia ossificans progressiva
55	Relapsing polychondritis
160	Congenital ichthyosis
286	Hereditary sideroblastic anemia
5	Progressive supranuclear palsy
156	Rett syndrome
140	Dorabe syndrome
144	Lennox-Gastaut syndrome
210	Single Ventricle
41	Giant cell arteritis
56	Behcet disease
218	Alport syndrome
49	Systemic lupus erythematosus
1	Spinal and bulbar muscular atrophy
10	Charcot-Marie-Tooth disease
63	Idiopathic thrombocytopenic purpura
45	Eosinophilic granulomatosis with Polyangiitis
215	Tetralogy of Fallot
225	Congenital nephrogenic diabetes insipidus
95	Autoimmune hepatitis
234	Peroxisomal disease (except Adrenoleukodystrophy)
81	Congenital adrenal hyperplasia
162	Pemphigoid
231	Alpha-1-antitrypsin deficiency
93	Primary biliary cholangitis
17	Multiple system atrophy
284	Diamond-Blackfan anemia
20	Adrenoleukodystrophy
274	Osteogenesis Imperfecta
280	Huge arteriovenous malformation with cervicofacial or limb lesion
19	Lysosomal storage disease
40	Takayasu arteritis
337	Homocystinuria
8	Huntington disease
169	Menkes disease
170	Occipital horn syndrome
42	Polyarteritis nodosa
64	Thrombotic thrombocytopenic purpura
326	Osteopetrosis
22	Moyamoya disease
149	Hemiconvulsion hemiplegia epilepsy syndrome
285	Fanconi anemia
114	Non-dystrophic myotonia syndrome
283	Acquired pure red cell aplasia
62	Paroxysmal nocturnal hemoglobinuria
60	Aplastic anemia
88	Chronic thromboembolic pulmonary hypertension
61	Autoimmune hemolytic anemia
102	Rubinstein-Taybi syndrome
89	Lymphangioleiomyomatosis
206	Fragile X syndrome
331	Idiopathic multicentric castleman disease
118	Myelomeningocele
288	Autoimmune acquired coagulation factor deficiency
271	Ankylosing spondylitis
106	Cryopyrin-associated periodic syndrome
251	Urea cycle disorder
108	TNF receptor-associated periodic syndrome
267	Hyper-IgD syndrome