Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Pulmonary embolism with pulmonary infarction
1 0 1 1.9E-02 0 0
CUI: C0036219
Disease: Sarcoma, Jensen
Sarcoma, Jensen
1 0 1 1.9E-02 0 0
CUI: C0149882
Disease: Acute esophagitis
Acute esophagitis
1 0 1 1.9E-02 0 0
CUI: C0155820
Disease: Acute bronchitis and bronchiolitis
Acute bronchitis and bronchiolitis
1 0 1 1.9E-02 0 0
CUI: C0235915
Disease: Pulmonary malformation
Pulmonary malformation
1 0 1 1.9E-02 0 0
CUI: C0265878
Disease: Preductal coarctation of aorta
Preductal coarctation of aorta
1 0 1 1.9E-02 0 0
CUI: C0266445
Disease: Congenital atresia of vas deferens
Congenital atresia of vas deferens
1 0 1 1.9E-02 0 0
CUI: C0268875
Disease: Urethrorectal fistula
Urethrorectal fistula
1 0 1 1.9E-02 0 0
CUI: C0271932
Disease: Anemia of chronic renal failure
Anemia of chronic renal failure
1 0 1 1.9E-02 0 0
CUI: C0332882
Disease: congenital obstruction
congenital obstruction
1 0 1 1.9E-02 0 0
CUI: C0333319
Disease: Involucrum
Involucrum
1 0 1 1.9E-02 0 0
CUI: C0333992
Disease: Acanthoma, Clear Cell
Acanthoma, Clear Cell
1 0 1 1.9E-02 0 0
CUI: C0338562
Disease: Sciatic nerve compression
Sciatic nerve compression
1 0 1 1.9E-02 0 0
CUI: C0339512
Disease: Bull's eye macular dystrophy
Bull's eye macular dystrophy
1 0 1 1.9E-02 0 0
CUI: C0340037
Disease: Young Syndrome
Young Syndrome
1 0 1 1.9E-02 0 0
CUI: C0343440
Disease: Pulmonary melioidosis
Pulmonary melioidosis
1 0 1 1.9E-02 0 0
CUI: C0392445
Disease: Necrobiosis Lipoidica Diabeticorum
Necrobiosis Lipoidica Diabeticorum
1 0 1 1.9E-02 0 0
Distal intestinal obstruction syndrome
1 0 1 1.9E-02 0 0
CUI: C0403819
Disease: Acquired obstructive azoospermia
Acquired obstructive azoospermia
1 0 1 1.9E-02 0 0
CUI: C0431603
Disease: Ectopic liver
Ectopic liver
1 0 1 1.9E-02 0 0
CUI: C0472713
Disease: Anemia of renal disease
Anemia of renal disease
1 0 1 1.9E-02 0 0
Other congenital malformation syndromes with other skeletal changes
1 0 1 1.9E-02 0 0
CUI: C0543645
Disease: Heterozygous hemoglobinopathy
Heterozygous hemoglobinopathy
1 0 1 1.9E-02 0 0
CUI: C0578736
Disease: Inguinal lymphadenopathy
Inguinal lymphadenopathy
1 0 1 1.9E-02 0 0
CUI: C0595928
Disease: Serum calcium increased
Serum calcium increased
1 0 1 1.9E-02 0 0