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: C0001828
Disease: Agricultural Workers' Diseases
Agricultural Workers' Diseases
1 0 1 2.1E-02 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect
1 0 1 2.1E-02 0 0
CUI: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms
1 0 1 2.1E-02 0 0
CUI: C0014127
Disease: Endocervicitis
Endocervicitis
1 0 1 2.1E-02 0 0
CUI: C0014541
Disease: Epiglottitis
Epiglottitis
1 0 1 2.1E-02 0 0
CUI: C0014574
Disease: Epiphysitis
Epiphysitis
1 0 1 2.1E-02 0 0
CUI: C0023119
Disease: Lathyrism
Lathyrism
1 0 1 2.1E-02 0 0
CUI: C0025211
Disease: Conjunctival melanosis
Conjunctival melanosis
1 0 1 2.1E-02 0 0
CUI: C0031085
Disease: Periodontal Abscess
Periodontal Abscess
1 0 1 2.1E-02 0 0
CUI: C0032044
Disease: Placenta Accreta
Placenta Accreta
1 0 1 2.1E-02 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma
1 0 1 2.1E-02 0 0
CUI: C0085313
Disease: Blastocystis Infections
Blastocystis Infections
1 0 1 2.1E-02 0 0
CUI: C0085388
Disease: Intracranial Tuberculoma
Intracranial Tuberculoma
1 0 1 2.1E-02 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia
1 0 1 2.1E-02 0 0
CUI: C0154298
Disease: Acute posthaemorrhagic anaemia
Acute posthaemorrhagic anaemia
1 0 1 2.1E-02 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers
1 0 1 2.1E-02 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe
1 0 1 2.1E-02 0 0
CUI: C0158784
Disease: Accessory skeletal muscle
Accessory skeletal muscle
1 0 1 2.1E-02 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis
1 0 1 2.1E-02 0 0
CUI: C0238309
Disease: Ischemic peripheral neuropathy
Ischemic peripheral neuropathy
1 0 1 2.1E-02 0 0
CUI: C0238814
Disease: brain hemangioma
brain hemangioma
1 0 1 2.1E-02 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus
1 0 1 2.1E-02 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome
1 0 1 2.1E-02 0 0
Congenital absence of pulmonic valve
1 0 1 2.1E-02 0 0
CUI: C0265974
Disease: Birthmark
Birthmark
1 0 1 2.1E-02 0 0