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: C0023786
Disease: Mucopolysaccharidosis I
Mucopolysaccharidosis I
0 31 0 0 2 1.3E-02
CUI: C0026918
Disease: Mycobacterium Infections
Mycobacterium Infections
0 14 0 0 1 7.0E-03
CUI: C0473527
Disease: Hypoalphalipoproteinemias
Hypoalphalipoproteinemias
0 7 0 0 1 7.4E-03
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen
0 6 0 0 1 7.5E-03
CUI: C2350529
Disease: Pulmonary Aspergillosis
Pulmonary Aspergillosis
0 4 0 0 1 7.6E-03
CUI: C2350530
Disease: Bronchopulmonary Aspergillosis
Bronchopulmonary Aspergillosis
0 4 0 0 1 7.6E-03
CUI: C0031557
Disease: Phlegmon
Phlegmon
1 0 1 3.8E-02 0 0
CUI: C0155526
Disease: Cochlear otosclerosis
Cochlear otosclerosis
1 0 1 3.8E-02 0 0
CUI: C0221069
Disease: Anterior Spinal Artery Syndrome
Anterior Spinal Artery Syndrome
1 0 1 3.8E-02 0 0
CUI: C0235584
Disease: Granulocytopenia severe
Granulocytopenia severe
1 0 1 3.8E-02 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm
1 0 1 3.8E-02 0 0
Knuckle pads, leuconychia and sensorineural deafness
1 0 1 3.8E-02 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia
1 0 1 3.8E-02 0 0
CUI: C0268276
Disease: Juvenile GM 2 gangliosidosis
Juvenile GM 2 gangliosidosis
1 2 1 3.8E-02 2 1.6E-02
CUI: C0268278
Disease: Infantile GM 2 gangliosidosis
Infantile GM 2 gangliosidosis
1 0 1 3.8E-02 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome
1 0 1 3.8E-02 0 0
CUI: C0276839
Disease: Infection by Cytauxzoon
Infection by Cytauxzoon
1 0 1 3.8E-02 0 0
CUI: C0280301
Disease: Hard Palate Squamous Cell Carcinoma
Hard Palate Squamous Cell Carcinoma
1 0 1 3.8E-02 0 0
CUI: C0282220
Disease: Amaurotic Familial Idiocy
Amaurotic Familial Idiocy
1 0 1 3.8E-02 0 0
CUI: C0333419
Disease: Sarcoid type granuloma
Sarcoid type granuloma
1 0 1 3.8E-02 0 0
CUI: C0392322
Disease: Undifferentiated schizophrenia
Undifferentiated schizophrenia
1 0 1 3.8E-02 0 0
Hearing loss associated with syndrome
1 0 1 3.8E-02 0 0
CUI: C0401067
Disease: Unilateral inguinal hernia NOS
Unilateral inguinal hernia NOS
1 0 1 3.8E-02 0 0
CUI: C0473577
Disease: Eccrine nevus
Eccrine nevus
1 0 1 3.8E-02 0 0
Porokeratotic eccrine ostial and dermal duct nevus
1 0 1 3.8E-02 0 0