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: C0206369
Disease: Splenosis
Splenosis 		3 0 1 0.11 0 0
CUI: C1328551
Disease: Transfusion associated graft versus host disease
Transfusion associated graft versus host disease 		3 0 1 0.11 0 0
CUI: C1504533
Disease: Post transplant erythrocytosis
Post transplant erythrocytosis 		3 0 1 0.11 0 0
CUI: C1836727
Disease: Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease 		3 0 1 0.11 0 0
CUI: C2359904
Disease: Aggregated erythrocytes
Aggregated erythrocytes 		3 0 1 0.11 0 0
CUI: C4025283
Disease: Compensated hemolytic anemia
Compensated hemolytic anemia 		3 0 1 0.11 0 0
CUI: C0038475
Disease: Double structure
Double structure 		4 0 1 1.0E-01 0 0
CUI: C0272048
Disease: stomatocytic anemia
stomatocytic anemia 		15 0 2 1.0E-01 0 0
CUI: C0345319
Disease: Cyst of hydatid of Morgagni
Cyst of hydatid of Morgagni 		4 0 1 1.0E-01 0 0
CUI: C0854258
Disease: Pseudoprecocious puberty
Pseudoprecocious puberty 		4 0 1 1.0E-01 0 0
CUI: C1843168
Disease: Myelin outfoldings
Myelin outfoldings 		4 0 1 1.0E-01 0 0
CUI: C3888087
Disease: Charcot-Marie-Tooth disease, Type 2I
Charcot-Marie-Tooth disease, Type 2I 		4 14 1 1.0E-01 1 6.7E-02
CUI: C4025610
Disease: Peripheral dysmyelination
Peripheral dysmyelination 		4 0 1 1.0E-01 0 0
CUI: C0002881
Disease: Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital 		27 0 3 9.7E-02 0 0
CUI: C0020058
Disease: Howell-Jolly Bodies
Howell-Jolly Bodies 		5 0 1 9.1E-02 0 0
CUI: C0027743
Disease: Nerve compression syndrome
Nerve compression syndrome 		5 0 1 9.1E-02 0 0
CUI: C0221409
Disease: Anemia, hereditary spherocytic hemolytic
Anemia, hereditary spherocytic hemolytic 		5 0 1 9.1E-02 0 0
CUI: C0553720
Disease: Spherocytosis
Spherocytosis 		5 0 1 9.1E-02 0 0
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor 		5 1 1 9.1E-02 1 0.50
CUI: C1510429
Disease: Entrapment Neuropathies
Entrapment Neuropathies 		5 0 1 9.1E-02 0 0
CUI: C1864498
Disease: RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE
RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE 		5 0 1 9.1E-02 0 0
CUI: C1970028
Disease: MALARIA, SUSCEPTIBILITY TO (finding)
MALARIA, SUSCEPTIBILITY TO (finding) 		5 0 1 9.1E-02 0 0
CUI: C4722277
Disease: NEUROPATHY, CONGENITAL HYPOMYELINATING, 2
NEUROPATHY, CONGENITAL HYPOMYELINATING, 2 		5 0 1 9.1E-02 0 0
CUI: C0005806
Disease: Blood Group Incompatibility
Blood Group Incompatibility 		6 0 1 8.3E-02 0 0
CUI: C0019816
Disease: Hereditary, Type VII, Motor and Sensory Neuropathy
Hereditary, Type VII, Motor and Sensory Neuropathy 		6 0 1 8.3E-02 0 0