Source: INFERRED ×
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: C0009806
Disease: Constipation
Constipation 		289 0 1 3.5E-03 0 0
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		196 0 1 5.1E-03 0 0
CUI: C0011334
Disease: Dental caries
Dental caries 		191 0 1 5.2E-03 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism 		1039 0 1 9.6E-04 0 0
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		734 0 1 1.4E-03 0 0
CUI: C0015672
Disease: Fatigue
Fatigue 		340 0 1 2.9E-03 0 0
CUI: C0015967
Disease: Fever
Fever 		239 0 1 4.2E-03 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot 		282 0 1 3.5E-03 0 0
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		308 0 1 3.2E-03 0 0
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic 		13 0 1 7.7E-02 0 0
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		681 0 1 1.5E-03 0 0
CUI: C0023518
Disease: Leukocytosis
Leukocytosis 		51 0 1 2.0E-02 0 0
CUI: C0027022
Disease: Myeloproliferative disease
Myeloproliferative disease 		15 0 1 6.7E-02 0 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		773 0 1 1.3E-03 0 0
CUI: C0038002
Disease: Splenomegaly
Splenomegaly 		326 0 1 3.1E-03 0 0
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia 		252 0 1 4.0E-03 0 0
CUI: C0040433
Disease: Tooth Crowding
Tooth Crowding 		82 0 1 1.2E-02 0 0
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly 		109 0 1 9.2E-03 0 0
CUI: C0232462
Disease: Decrease in appetite
Decrease in appetite 		33 0 1 3.0E-02 0 0
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate 		496 0 1 2.0E-03 0 0
CUI: C0265610
Disease: Clinodactyly of fingers
Clinodactyly of fingers 		152 0 1 6.6E-03 0 0
CUI: C0423224
Disease: Sunken eyes
Sunken eyes 		171 0 1 5.8E-03 0 0
CUI: C0426422
Disease: Narrow nose
Narrow nose 		17 0 1 5.9E-02 0 0
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		593 0 1 1.7E-03 0 0
CUI: C0544886
Disease: Somatic mutation
Somatic mutation 		151 0 1 6.6E-03 0 0