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: C0024967
Disease: Maximal Voluntary Ventilation
Maximal Voluntary Ventilation
0 3 0 0 2 2.7E-03
CUI: C0007862
Disease: Cervico-Brachial Neuralgia
Cervico-Brachial Neuralgia
1 0 1 2.3E-03 0 0
CUI: C0008521
Disease: Choroid Diseases
Choroid Diseases
1 0 1 2.3E-03 0 0
CUI: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms
1 0 1 2.3E-03 0 0
CUI: C0015338
Disease: Exstrophy
Exstrophy
1 0 1 2.3E-03 0 0
CUI: C0017570
Disease: Gingival Neoplasms
Gingival Neoplasms
1 0 1 2.3E-03 0 0
CUI: C0023119
Disease: Lathyrism
Lathyrism
1 0 1 2.3E-03 0 0
CUI: C0031925
Disease: Pilonidal Cyst
Pilonidal Cyst
1 0 1 2.3E-03 0 0
CUI: C0033735
Disease: Protothecosis
Protothecosis
1 0 1 2.3E-03 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma
1 0 1 2.3E-03 0 0
CUI: C0036413
Disease: Scleredema Adultorum
Scleredema Adultorum
1 0 1 2.3E-03 0 0
CUI: C0038557
Disease: Submandibular Gland Diseases
Submandibular Gland Diseases
1 0 1 2.3E-03 0 0
CUI: C0039614
Disease: Tetanus
Tetanus
1 0 1 2.3E-03 0 0
CUI: C0040947
Disease: Trichostrongyloidiasis
Trichostrongyloidiasis
1 0 1 2.3E-03 0 0
CUI: C0085920
Disease: Brachial Neuralgia
Brachial Neuralgia
1 0 1 2.3E-03 0 0
Megaloblastic anemia due to folate deficiency
1 0 1 2.3E-03 0 0
CUI: C0151604
Disease: Genital Edema
Genital Edema
1 0 1 2.3E-03 0 0
CUI: C0151772
Disease: Manic psychosis
Manic psychosis
1 0 1 2.3E-03 0 0
CUI: C0158360
Disease: Fibromatosis, Plantar
Fibromatosis, Plantar
1 0 1 2.3E-03 0 0
Aplasia of Lacrimal and Salivary Glands
1 0 1 2.3E-03 0 0
CUI: C0159104
Disease: Electrooculogram abnormal
Electrooculogram abnormal
1 0 1 2.3E-03 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis
1 0 1 2.3E-03 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement
1 0 1 2.3E-03 0 0
CUI: C0202363
Disease: Cotinine measurement
Cotinine measurement
1 0 1 2.3E-03 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type
1 0 1 2.3E-03 0 0