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: C0039614
Disease: Tetanus
Tetanus 		1 0 1 3.4E-02 0 0
CUI: C0398782
Disease: Carboxypeptidase N Deficiency
Carboxypeptidase N Deficiency 		1 1 1 3.4E-02 1 2.0E-02
CUI: C0555197
Disease: Florid cemento-osseous dysplasia
Florid cemento-osseous dysplasia 		1 0 1 3.4E-02 0 0
CUI: C0877061
Disease: Epiduritis
Epiduritis 		1 0 1 3.4E-02 0 0
CUI: C1265776
Disease: Diffuse telangiectasis
Diffuse telangiectasis 		1 0 1 3.4E-02 0 0
CUI: C1856453
Disease: Mild thrombocytopenia
Mild thrombocytopenia 		1 0 1 3.4E-02 0 0
CUI: C1969785
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder) 		1 0 1 3.4E-02 0 0
CUI: C3495361
Disease: Gigantiform Cementoma, Familial
Gigantiform Cementoma, Familial 		1 0 1 3.4E-02 0 0
CUI: C3714995
Disease: CARDIOMYOPATHY, DILATED, 1KK
CARDIOMYOPATHY, DILATED, 1KK 		1 0 1 3.4E-02 0 0
CUI: C3714998
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 22
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 22 		1 0 1 3.4E-02 0 0
CUI: C3807697
Disease: Bilateral foot drop
Bilateral foot drop 		1 0 1 3.4E-02 0 0
CUI: C3808963
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 4
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 4 		1 0 1 3.4E-02 0 0
CUI: C4225199
Disease: CARDIAC ARRHYTHMIA WITH INCREASED SERUM CREATINE KINASE
CARDIAC ARRHYTHMIA WITH INCREASED SERUM CREATINE KINASE 		1 0 1 3.4E-02 0 0
CUI: C4284588
Disease: SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE 		1 0 1 3.4E-02 0 0
CUI: C4324411
Disease: Blood type incompatibility
Blood type incompatibility 		1 0 1 3.4E-02 0 0
CUI: C4479186
Disease: NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE
NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE 		1 0 1 3.4E-02 0 0
CUI: C4703482
Disease: Severe Epstein Barr virus infection
Severe Epstein Barr virus infection 		1 0 1 3.4E-02 0 0
CUI: C0020701
Disease: Hysteria
Hysteria 		2 0 1 3.3E-02 0 0
CUI: C0158371
Disease: Acute osteomyelitis
Acute osteomyelitis 		2 0 1 3.3E-02 0 0
CUI: C0221289
Disease: Synovioma, benign
Synovioma, benign 		2 0 1 3.3E-02 0 0
CUI: C0268532
Disease: Deficiency of prolidase
Deficiency of prolidase 		2 0 1 3.3E-02 0 0
CUI: C0270202
Disease: Hemolytic disease of fetus OR newborn due to ABO immunization
Hemolytic disease of fetus OR newborn due to ABO immunization 		2 0 1 3.3E-02 0 0
CUI: C0424810
Disease: Periorbital swelling
Periorbital swelling 		2 0 1 3.3E-02 0 0
CUI: C0586738
Disease: Calf muscle weakness
Calf muscle weakness 		2 0 1 3.3E-02 0 0
CUI: C0750863
Disease: Finding of creatine kinase level
Finding of creatine kinase level 		2 2 2 6.9E-02 2 3.9E-02