Source: ALL
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: C0005806
Disease: Blood Group Incompatibility
Blood Group Incompatibility 		6 0 1 1.0E-01 0 0
CUI: C0042875
Disease: Vitamin E Deficiency
Vitamin E Deficiency 		6 0 1 1.0E-01 0 0
CUI: C0155550
Disease: Neural hearing loss
Neural hearing loss 		6 0 1 1.0E-01 0 0
CUI: C1862324
Disease: Elliptocytosis 4
Elliptocytosis 4 		6 0 1 1.0E-01 0 0
CUI: C0342162
Disease: Compensated hypothyroidism
Compensated hypothyroidism 		7 0 1 9.1E-02 0 0
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		7 0 1 9.1E-02 0 0
CUI: C2676974
Disease: Hypoplasia of the cochlea
Hypoplasia of the cochlea 		7 0 1 9.1E-02 0 0
CUI: C4025184
Disease: Spontaneous hemolytic crises
Spontaneous hemolytic crises 		7 0 1 9.1E-02 0 0
CUI: C1969073
Disease: Hyperchloremic metabolic acidosis
Hyperchloremic metabolic acidosis 		8 0 1 8.3E-02 0 0
CUI: C0013394
Disease: Dyspareunia (female)
Dyspareunia (female) 		9 0 1 7.7E-02 0 0
CUI: C0022681
Disease: Medullary sponge kidney
Medullary sponge kidney 		9 0 1 7.7E-02 0 0
CUI: C1849478
Disease: Increased red cell osmotic fragility
Increased red cell osmotic fragility 		9 0 1 7.7E-02 0 0
CUI: C4021553
Disease: Periodic hypokalemic paresis
Periodic hypokalemic paresis 		9 0 1 7.7E-02 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis 		52 0 4 7.5E-02 0 0
CUI: C4272578
Disease: Autosomal Recessive Osteopetrosis
Autosomal Recessive Osteopetrosis 		24 0 2 7.4E-02 0 0
CUI: C0392485
Disease: Congenital diverticulum of pharynx
Congenital diverticulum of pharynx 		10 0 1 7.1E-02 0 0
CUI: C3538946
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT
DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT 		10 0 1 7.1E-02 0 0
CUI: C3841459
Disease: Hb H disease
Hb H disease 		10 2 1 7.1E-02 1 7.1E-02
CUI: C0002881
Disease: Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital 		27 0 2 6.7E-02 0 0
CUI: C0427480
Disease: Elliptocytosis found
Elliptocytosis found 		12 0 1 6.2E-02 0 0
CUI: C0002889
Disease: Anemia, Microangiopathic
Anemia, Microangiopathic 		13 0 1 5.9E-02 0 0
CUI: C0029810
Disease: Other specified iron deficiency anemias
Other specified iron deficiency anemias 		13 0 1 5.9E-02 0 0
CUI: C0268435
Disease: Renal Tubular Acidosis, Type II
Renal Tubular Acidosis, Type II 		13 0 1 5.9E-02 0 0
CUI: C0677598
Disease: Stomatocytosis Result
Stomatocytosis Result 		13 0 1 5.9E-02 0 0
CUI: C4531297
Disease: Increased mean corpuscular hemoglobin concentration
Increased mean corpuscular hemoglobin concentration 		13 0 1 5.9E-02 0 0