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: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology
70 0 1 2.0E-03 0 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness
70 0 1 2.0E-03 0 0
CUI: C0020620
Disease: Hypohidrosis
Hypohidrosis
69 0 1 2.0E-03 0 0
CUI: C0020678
Disease: Hypotrichosis
Hypotrichosis
69 0 1 2.0E-03 0 0
CUI: C0240538
Disease: Convex nasal ridge
Convex nasal ridge
69 0 1 2.0E-03 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome
68 0 1 2.0E-03 0 0
CUI: C4282407
Disease: Sparse and thin eyebrow
Sparse and thin eyebrow
68 0 1 2.0E-03 0 0
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests
67 0 1 2.0E-03 0 0
Familial Nonmedullary Thyroid Cancer
66 0 1 2.0E-03 0 0
CUI: C0268237
Disease: Cytochrome-c Oxidase Deficiency
Cytochrome-c Oxidase Deficiency
65 0 1 2.0E-03 0 0
CUI: C0376705
Disease: Viral Load result
Viral Load result
65 0 1 2.0E-03 0 0
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result
65 0 1 2.0E-03 0 0
CUI: C2243051
Disease: Large head (disorder)
Large head (disorder)
64 0 1 2.0E-03 0 0
CUI: C0025037
Disease: Meckel Diverticulum
Meckel Diverticulum
63 0 1 2.0E-03 0 0
CUI: C0156394
Disease: Hypertrophy of clitoris
Hypertrophy of clitoris
63 0 1 2.0E-03 0 0
CUI: C0231687
Disease: Spastic gait
Spastic gait
62 0 1 2.0E-03 0 0
CUI: C0919677
Disease: Protein C measurement
Protein C measurement
62 0 1 2.0E-03 0 0
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement
62 0 1 2.0E-03 0 0
CUI: C4082304
Disease: Oligodontia
Oligodontia
62 0 1 2.0E-03 0 0
CUI: C4722327
Disease: PROSTATE CANCER, HEREDITARY, 1
PROSTATE CANCER, HEREDITARY, 1
62 0 1 2.0E-03 0 0
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL
61 0 1 2.0E-03 0 0
CUI: C0426817
Disease: Short ribs
Short ribs
60 0 1 2.0E-03 0 0
CUI: C1843300
Disease: Sparse eyelashes
Sparse eyelashes
60 0 1 2.0E-03 0 0
CUI: C1854418
Disease: Biparietal narrowing
Biparietal narrowing
60 0 1 2.0E-03 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
59 0 1 2.0E-03 0 0