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: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious
0 4 0 0 1 3.7E-02
Refractory anaemia with excess blasts
0 2 0 0 1 4.0E-02
CUI: C0030286
Disease: Pancreatic Diseases
Pancreatic Diseases
0 11 0 0 1 2.9E-02
CUI: C0153594
Disease: Malignant neoplasm of testis
Malignant neoplasm of testis
0 31 0 0 1 1.9E-02
CUI: C0162296
Disease: Polyarthralgia
Polyarthralgia
0 1 0 0 1 4.2E-02
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney
0 8 0 0 1 3.2E-02
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis
0 1 0 0 1 4.2E-02
CUI: C0525041
Disease: Neurobehavioral Manifestations
Neurobehavioral Manifestations
0 3 0 0 1 3.8E-02
CUI: C0702157
Disease: Thalassemia trait
Thalassemia trait
0 2 0 0 1 4.0E-02
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome
0 2 0 0 1 4.0E-02
CUI: C0854135
Disease: Pseudomonas aeruginosa infection
Pseudomonas aeruginosa infection
0 1 0 0 1 4.2E-02
Malignant Testicular Germ Cell Tumor
0 62 0 0 1 1.2E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous
0 2 0 0 1 4.0E-02
CUI: C0001261
Disease: Actinomycosis
Actinomycosis
1 0 1 4.8E-02 0 0
CUI: C0006542
Disease: Byssinosis
Byssinosis
1 0 1 4.8E-02 0 0
Panniculitis, Nodular Nonsuppurative
1 0 1 4.8E-02 0 0
CUI: C0241876
Disease: Obstructive emphysema
Obstructive emphysema
1 0 1 4.8E-02 0 0
CUI: C0263578
Disease: Riehl's melanosis
Riehl's melanosis
1 0 1 4.8E-02 0 0
CUI: C0266266
Disease: Congenital absence of pancreas
Congenital absence of pancreas
1 0 1 4.8E-02 0 0
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis
1 1 1 4.8E-02 1 4.2E-02
CUI: C0333295
Disease: Acute ulcer
Acute ulcer
1 0 1 4.8E-02 0 0
CUI: C0341248
Disease: Chronic duodenitis
Chronic duodenitis
1 0 1 4.8E-02 0 0
CUI: C0342856
Disease: Coproporphyria
Coproporphyria
1 0 1 4.8E-02 0 0
Homozygous acute intermittent porphyria
1 0 1 4.8E-02 0 0
CUI: C0342860
Disease: Homozygous variegate porphyria
Homozygous variegate porphyria
1 4 1 4.8E-02 3 0.12