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: C1619692
Disease: Nephrogenic Fibrosing Dermopathy
Nephrogenic Fibrosing Dermopathy
13 0 8 0.47 0 0
EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1
9 0 3 0.17 0 0
CUI: C0340908
Disease: Arteriovenous fistula stenosis
Arteriovenous fistula stenosis
3 0 2 0.15 0 0
CUI: C0158300
Disease: Adhesive Capsulitis
Adhesive Capsulitis
5 0 2 0.13 0 0
CUI: C0521626
Disease: Fibrosis of urinary bladder
Fibrosis of urinary bladder
5 0 2 0.13 0 0
CUI: C1842090
Disease: Platelet Glycoprotein IV Deficiency
Platelet Glycoprotein IV Deficiency
14 0 3 0.13 0 0
CUI: C0036216
Disease: Sarcoma, Experimental
Sarcoma, Experimental
7 0 2 0.12 0 0
CUI: C0264544
Disease: Adhesion of lung
Adhesion of lung
7 0 2 0.12 0 0
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
7 0 2 0.12 0 0
CUI: C0018179
Disease: Granular Dystrophy, Corneal
Granular Dystrophy, Corneal
8 0 2 0.11 0 0
CUI: C1442826
Disease: Neonatal necrotizing enterocolitis
Neonatal necrotizing enterocolitis
8 0 2 0.11 0 0
CUI: C0679408
Disease: Lesion of stomach
Lesion of stomach
9 0 2 0.11 0 0
CUI: C1260710
Disease: Acute ulcerative colitis
Acute ulcerative colitis
9 0 2 0.11 0 0
CUI: C1320638
Disease: Bone marrow myeloid dysplasia
Bone marrow myeloid dysplasia
9 0 2 0.11 0 0
CUI: C1334260
Disease: Intramuscular Myxoma
Intramuscular Myxoma
9 0 2 0.11 0 0
CUI: C1527383
Disease: Morphea
Morphea
20 0 3 0.10 0 0
CUI: C0085179
Disease: Eosinophilia-Myalgia Syndrome
Eosinophilia-Myalgia Syndrome
10 0 2 1.0E-01 0 0
CUI: C0339263
Disease: Pseudophakic corneal edema
Pseudophakic corneal edema
10 0 2 1.0E-01 0 0
CUI: C1262117
Disease: Fungal keratitis
Fungal keratitis
21 0 3 1.0E-01 0 0
CUI: C2267231
Disease: Chronic idiopathic neutropenia
Chronic idiopathic neutropenia
10 0 2 1.0E-01 0 0
CUI: C0016048
Disease: Fibromatosis
Fibromatosis
22 0 3 9.7E-02 0 0
CUI: C1314694
Disease: Astrocytoma, low grade
Astrocytoma, low grade
34 0 4 9.5E-02 0 0
CUI: C1510428
Disease: Cerebral abscess
Cerebral abscess
11 0 2 9.5E-02 0 0
CUI: C0403440
Disease: Thin basement membrane disease
Thin basement membrane disease
12 0 2 9.1E-02 0 0
Muscular dystrophy congenital, merosin negative
12 0 2 9.1E-02 0 0