Source: UNIPROT ×
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: C1832702
Disease: BRACHYDACTYLY, TYPE A2
BRACHYDACTYLY, TYPE A2 		2 0 1 1.8E-02 0 0
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE 		1 0 1 1.9E-02 0 0
CUI: C1839333
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 		1 0 1 1.9E-02 0 0
CUI: C1840390
Disease: Pseudohypoaldosteronism, Type IIb
Pseudohypoaldosteronism, Type IIb 		1 0 1 1.9E-02 0 0
CUI: C1846385
Disease: FOCAL CORTICAL DYSPLASIA OF TAYLOR
FOCAL CORTICAL DYSPLASIA OF TAYLOR 		3 0 1 1.8E-02 0 0
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g 		1 0 1 1.9E-02 0 0
CUI: C1861065
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9 		1 0 1 1.9E-02 0 0
CUI: C1863599
Disease: Hereditary Myopathy with Early Respiratory Failure
Hereditary Myopathy with Early Respiratory Failure 		1 0 1 1.9E-02 0 0
CUI: C1865871
Disease: HEMANGIOMA, CAPILLARY INFANTILE
HEMANGIOMA, CAPILLARY INFANTILE 		2 0 1 1.8E-02 0 0
CUI: C1866293
Disease: Retinal cone dystrophy 2
Retinal cone dystrophy 2 		1 0 1 1.9E-02 0 0
CUI: C2931258
Disease: Amaurosis congenita of Leber, type 1
Amaurosis congenita of Leber, type 1 		1 0 1 1.9E-02 0 0
CUI: C2939175
Disease: Meconium ileus
Meconium ileus 		1 0 1 1.9E-02 0 0
CUI: C3165106
Disease: Infiltrating duct carcinoma of female breast
Infiltrating duct carcinoma of female breast 		21 0 3 4.2E-02 0 0
CUI: C3552634
Disease: LYMPHOPROLIFERATIVE SYNDROME 1
LYMPHOPROLIFERATIVE SYNDROME 1 		1 0 1 1.9E-02 0 0
CUI: C3553270
Disease: DIARRHEA 6
DIARRHEA 6 		1 0 1 1.9E-02 0 0
CUI: C4014361
Disease: ABDOMINAL OBESITY-METABOLIC SYNDROME 3
ABDOMINAL OBESITY-METABOLIC SYNDROME 3 		1 0 1 1.9E-02 0 0
CUI: C4014833
Disease: IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES
IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES 		1 0 1 1.9E-02 0 0
CUI: C4015156
Disease: MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE 		1 0 1 1.9E-02 0 0
CUI: C4048328
Disease: cervical cancer
cervical cancer 		3 0 1 1.8E-02 0 0
CUI: C4225183
Disease: BRACHYDACTYLY, TYPE A1, D
BRACHYDACTYLY, TYPE A1, D 		1 0 1 1.9E-02 0 0
CUI: C4225259
Disease: SMITH-KINGSMORE SYNDROME
SMITH-KINGSMORE SYNDROME 		1 0 1 1.9E-02 0 0
CUI: C4225360
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30 		1 0 1 1.9E-02 0 0
CUI: C4225404
Disease: ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE
ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE 		1 0 1 1.9E-02 0 0
CUI: C4225418
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC 33
MENTAL RETARDATION, X-LINKED, SYNDROMIC 33 		1 0 1 1.9E-02 0 0
CUI: C4310629
Disease: LYMPHATIC MALFORMATION 7
LYMPHATIC MALFORMATION 7 		1 0 1 1.9E-02 0 0