Gene

Disease ID	Name
2	Amyotrophic lateral sclerosis
6	Parkinson disease
11	Myasthenia gravis
13	Multiple sclerosis/Neuromyelitis optica
36	Epidermolysis bullosa
46	Malignant rheumatoid arthritis
49	Systemic lupus erythematosus
50	Dermatomyositis
51	Scleroderma
53	Sjogren syndrome
56	Behcet disease
60	Aplastic anemia
61	Autoimmune hemolytic anemia
62	Paroxysmal nocturnal hemoglobinuria
65	Primary immunodeficiency
66	IgA nephropathy
85	Idiopathic interstitial pneumonia
95	Autoimmune hepatitis
96	Crohn disease
97	Ulcerative colitis
113	Muscular dystrophy
151	Rasmussen encephalitis
158	Tuberous sclerosis
164	Oculocutaneous albinism
222	Primary nephrotic syndrome
224	Purpura nephritis
226	Interstitial cystitis with Hunners ulcer
227	Osler disease
228	Bronchiolitis obliterans
283	Acquired pure red cell aplasia
284	Diamond-Blackfan anemia
285	Fanconi anemia
286	Hereditary sideroblastic anemia
299	Cystic fibrosis

[44] 11, 19, 20, 26, 28, 36, 38, 39, 40, 41, 42, 45, 46, 49, 50, 53, 55, 56, 58, 60, 61, 62, 63, 64, ...

Disease ID	Name
11	Myasthenia gravis
19	Lysosomal storage disease
20	Adrenoleukodystrophy
26	HTLV-1-associated myelopathy
28	Systemic amyloidosis
36	Epidermolysis bullosa
38	Stevens-Johnson syndrome
39	Toxic epidermal necrolysis
40	Takayasu arteritis
41	Giant cell arteritis
42	Polyarteritis nodosa
45	Eosinophilic granulomatosis with Polyangiitis
46	Malignant rheumatoid arthritis
49	Systemic lupus erythematosus
50	Dermatomyositis
53	Sjogren syndrome
55	Relapsing polychondritis
56	Behcet disease
58	Hypertrophic cardiomyopathy
60	Aplastic anemia
61	Autoimmune hemolytic anemia
62	Paroxysmal nocturnal hemoglobinuria
63	Idiopathic thrombocytopenic purpura
64	Thrombotic thrombocytopenic purpura
65	Primary immunodeficiency
90	Retinitis pigmentosa
93	Primary biliary cholangitis
95	Autoimmune hepatitis
97	Ulcerative colitis
107	Juvenile idiopathic arthritis
113	Muscular dystrophy
162	Pemphigoid
164	Oculocutaneous albinism
222	Primary nephrotic syndrome
226	Interstitial cystitis with Hunners ulcer
228	Bronchiolitis obliterans
234	Peroxisomal disease (except Adrenoleukodystrophy)
269	Pyogenic arthritis
274	Osteogenesis Imperfecta
283	Acquired pure red cell aplasia
284	Diamond-Blackfan anemia
285	Fanconi anemia
302	Leber hereditary optic neuropathy
326	Osteopetrosis

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