Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
394 96 50 8.5E-02 3 2.1E-02
Congenital arteriovenous malformation
127 0 29 8.4E-02 0 0
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases
399 0 50 8.4E-02 0 0
TNF receptor-associated periodic fever syndrome (TRAPS)
90 0 26 8.4E-02 0 0
CUI: C0035344
Disease: Retinopathy of Prematurity
Retinopathy of Prematurity
196 15 34 8.3E-02 3 5.0E-02
Amaurosis congenita of Leber, type 1
80 27 25 8.3E-02 2 2.7E-02
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome
421 0 51 8.3E-02 0 0
CUI: C0234251
Disease: Inflammatory pain
Inflammatory pain
266 0 39 8.2E-02 0 0
CUI: C0221505
Disease: Lesion of brain
Lesion of brain
188 9 33 8.2E-02 2 3.6E-02
CUI: C2936719
Disease: Mechanical Allodynia
Mechanical Allodynia
362 0 46 8.2E-02 0 0
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
616 390 65 8.1E-02 4 9.2E-03
CUI: C0027809
Disease: Neurilemmoma
Neurilemmoma
178 0 32 8.1E-02 0 0
CUI: C0872084
Disease: Sarcopenia
Sarcopenia
152 0 30 8.1E-02 0 0
CUI: C0399440
Disease: Hereditary gingival fibromatosis
Hereditary gingival fibromatosis
86 0 25 8.1E-02 0 0
CUI: C0003864
Disease: Arthritis
Arthritis
992 66 93 8.1E-02 2 1.8E-02
CUI: C0234985
Disease: Mental deterioration
Mental deterioration
407 90 49 8.1E-02 3 2.2E-02
Respiratory Distress Syndrome, Newborn
143 37 29 8.0E-02 1 1.2E-02
CUI: C0740391
Disease: Middle Cerebral Artery Occlusion
Middle Cerebral Artery Occlusion
607 0 63 8.0E-02 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis
66 22 23 7.9E-02 2 2.9E-02
CUI: C4722099
Disease: High grade glioma
High grade glioma
190 0 32 7.9E-02 0 0
CUI: C0240066
Disease: Iron deficiency
Iron deficiency
179 0 31 7.8E-02 0 0
CUI: C0017601
Disease: Glaucoma
Glaucoma
511 112 55 7.8E-02 1 6.3E-03
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
1069 411 95 7.8E-02 1 2.2E-03
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss
141 0 28 7.8E-02 0 0
CUI: C0011269
Disease: Dementia, Vascular
Dementia, Vascular
197 25 32 7.8E-02 1 1.4E-02