Source: CURATED ×
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: C0009759
Disease: Conjunctival Diseases
Conjunctival Diseases 		1 0 1 7.6E-03 0 0
CUI: C0023531
Disease: Leukoplakia
Leukoplakia 		1 0 1 7.6E-03 0 0
CUI: C0024894
Disease: Mastitis
Mastitis 		1 0 1 7.6E-03 0 0
CUI: C0035021
Disease: Relapsing Fever
Relapsing Fever 		1 0 1 7.6E-03 0 0
CUI: C0036429
Disease: Sclerosis
Sclerosis 		1 0 1 7.6E-03 0 0
CUI: C0085568
Disease: Buruli Ulcer
Buruli Ulcer 		1 0 1 7.6E-03 0 0
CUI: C0242666
Disease: Protein S Deficiency
Protein S Deficiency 		1 0 1 7.6E-03 0 0
CUI: C0472817
Disease: WHIM syndrome
WHIM syndrome 		1 0 1 7.6E-03 0 0
CUI: C0497156
Disease: Lymphadenopathy
Lymphadenopathy 		1 0 1 7.6E-03 0 0
CUI: C0524988
Disease: Schnitzler Syndrome
Schnitzler Syndrome 		1 0 1 7.6E-03 0 0
CUI: C1333813
Disease: Central Nervous System Germinoma
Central Nervous System Germinoma 		1 0 1 7.6E-03 0 0
CUI: C1512709
Disease: Chronic Lymphoproliferative Disorder of NK-Cells
Chronic Lymphoproliferative Disorder of NK-Cells 		1 0 1 7.6E-03 0 0
CUI: C1704317
Disease: Leukokeratosis
Leukokeratosis 		1 0 1 7.6E-03 0 0
CUI: C1832392
Disease: DIABETES MELLITUS, INSULIN-DEPENDENT, 12
DIABETES MELLITUS, INSULIN-DEPENDENT, 12 		1 0 1 7.6E-03 0 0
CUI: C1834176
Disease: MYELOKATHEXIS, ISOLATED
MYELOKATHEXIS, ISOLATED 		1 0 1 7.6E-03 0 0
CUI: C1838329
Disease: APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS
APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS 		1 0 1 7.6E-03 0 0
CUI: C1838656
Disease: Macrocytosis, Familial
Macrocytosis, Familial 		1 0 1 7.6E-03 0 0
CUI: C1847532
Disease: MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET
MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET 		1 0 1 7.6E-03 0 0
CUI: C1849157
Disease: Resistance to Insulin-Like Growth Factor I
Resistance to Insulin-Like Growth Factor I 		1 0 1 7.6E-03 0 0
CUI: C1850808
Disease: Miyoshi myopathy
Miyoshi myopathy 		1 0 1 7.6E-03 0 0
CUI: C1850889
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B 		1 0 1 7.6E-03 0 0
CUI: C1853566
Disease: Genitopatellar Syndrome
Genitopatellar Syndrome 		1 0 1 7.6E-03 0 0
CUI: C1860991
Disease: NOONAN SYNDROME 3
NOONAN SYNDROME 3 		1 0 1 7.6E-03 0 0
CUI: C1863557
Disease: Young Simpson syndrome
Young Simpson syndrome 		1 0 1 7.6E-03 0 0
CUI: C2673648
Disease: Hypomagnesemia 4, Renal
Hypomagnesemia 4, Renal 		1 0 1 7.6E-03 0 0