Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Embolic Infarction, Middle Cerebral Artery
35 0 1 2.8E-02 0 0
Thrombotic Infarction, Middle Cerebral Artery
35 0 1 2.8E-02 0 0
Right Middle Cerebral Artery Infarction
35 0 1 2.8E-02 0 0
Mycosis fungoides/Sezary syndrome NOS
36 0 1 2.7E-02 0 0
CUI: C0426818
Disease: Thin rib
Thin rib
42 0 1 2.3E-02 0 0
CUI: C1836308
Disease: Generalized joint laxity
Generalized joint laxity
44 0 1 2.2E-02 0 0
CUI: C1849075
Disease: Relative macrocephaly
Relative macrocephaly
49 0 1 2.0E-02 0 0
CUI: C0014118
Disease: Endocarditis
Endocarditis
56 0 1 1.8E-02 0 0
CUI: C0023529
Disease: Leukomalacia, Periventricular
Leukomalacia, Periventricular
62 0 1 1.6E-02 0 0
CUI: C1541923
Disease: Infective endocarditis
Infective endocarditis
62 0 1 1.6E-02 0 0
CUI: C0014121
Disease: Bacterial Endocarditis
Bacterial Endocarditis
68 0 1 1.4E-02 0 0
CUI: C0271160
Disease: Cortical cataract
Cortical cataract
69 0 1 1.4E-02 0 0
CUI: C0542514
Disease: Blue sclera
Blue sclera
70 0 1 1.4E-02 0 0
CUI: C0005956
Disease: Bone Marrow Diseases
Bone Marrow Diseases
84 0 1 1.2E-02 0 0
CUI: C0037928
Disease: Spinal Cord Diseases
Spinal Cord Diseases
84 0 1 1.2E-02 0 0
CUI: C0399440
Disease: Hereditary gingival fibromatosis
Hereditary gingival fibromatosis
86 0 1 1.1E-02 0 0
CUI: C0030481
Disease: Tropical Spastic Paraparesis
Tropical Spastic Paraparesis
88 0 1 1.1E-02 0 0
CUI: C0079680
Disease: Lentivirus Infections
Lentivirus Infections
88 0 1 1.1E-02 0 0
CUI: C0029434
Disease: Osteogenesis Imperfecta
Osteogenesis Imperfecta
90 0 1 1.1E-02 0 0
CUI: C1844704
Disease: Platyspondyly
Platyspondyly
93 0 1 1.1E-02 0 0
CUI: C0026946
Disease: Mycoses
Mycoses
94 0 1 1.1E-02 0 0
CUI: C0022116
Disease: Ischemia
Ischemia
103 0 1 9.6E-03 0 0
CUI: C0025995
Disease: Micromelia
Micromelia
104 0 1 9.5E-03 0 0
CUI: C1839758
Disease: Narrow forehead
Narrow forehead
106 0 1 9.3E-03 0 0
CUI: C1456868
Disease: Diabetic foot ulcer
Diabetic foot ulcer
107 0 1 9.3E-03 0 0