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: C0026961
Disease: Mydriasis
Mydriasis
0 2 0 0 1 9.1E-02
CUI: C0240595
Disease: Rotary Nystagmus
Rotary Nystagmus
0 3 0 0 1 8.3E-02
CUI: C0426209
Disease: amniotic fluid meconium stained
amniotic fluid meconium stained
0 4 0 0 1 7.7E-02
Primitive reflexes (palmomental, snout, glabellar)
0 1 0 0 1 1.0E-01
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
0 10 0 0 1 5.3E-02
CUI: C1845274
Disease: Abnormal conjugate eye movement
Abnormal conjugate eye movement
0 5 0 0 1 7.1E-02
CUI: C1849043
Disease: Soft, doughy skin
Soft, doughy skin
0 4 0 0 1 7.7E-02
CUI: C1857479
Disease: Short columella
Short columella
0 5 0 0 1 7.1E-02
CUI: C1859481
Disease: Abnormal finger flexion creases
Abnormal finger flexion creases
0 1 0 0 1 1.0E-01
CUI: C1969810
Disease: FEBRILE CONVULSIONS, FAMILIAL, 8
FEBRILE CONVULSIONS, FAMILIAL, 8
0 13 0 0 1 4.5E-02
CUI: C4021603
Disease: Widely spaced primary teeth
Widely spaced primary teeth
0 1 0 0 1 1.0E-01
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 4.8E-03 0 0
CUI: C0000921
Disease: Accidental Falls
Accidental Falls
22 0 1 6.0E-03 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia
46 0 1 5.3E-03 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic
209 0 1 2.8E-03 0 0
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome
243 0 1 2.6E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
20 0 1 6.1E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic
11 0 1 6.5E-03 0 0
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
435 0 1 1.7E-03 0 0
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis
130 0 1 3.6E-03 0 0
CUI: C0001420
Disease: Papillary adenocarcinoma
Papillary adenocarcinoma
11 0 1 6.5E-03 0 0
CUI: C0001442
Disease: Adenosarcoma
Adenosarcoma
9 0 1 6.5E-03 0 0
CUI: C0001486
Disease: Adenovirus Infections
Adenovirus Infections
145 0 1 3.5E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders
9 0 1 6.5E-03 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia
87 0 1 4.3E-03 0 0