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: C0270736
Disease: Essential Tremor
Essential Tremor
122 0 1 3.2E-03 0 0
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth
122 0 1 3.2E-03 0 0
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay
118 0 1 3.2E-03 0 0
CUI: C0266617
Disease: Congenital anomaly of face
Congenital anomaly of face
114 0 1 3.2E-03 0 0
CUI: C0231712
Disease: Waddling gait
Waddling gait
113 0 1 3.2E-03 0 0
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies
104 0 1 3.3E-03 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology
104 0 1 3.3E-03 0 0
Corpuscular Hemoglobin Concentration Mean
401 0 2 3.4E-03 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin
101 0 1 3.4E-03 0 0
CUI: C1840379
Disease: Cerebellar vermis hypoplasia
Cerebellar vermis hypoplasia
100 0 1 3.4E-03 0 0
CUI: C0037369
Disease: Smoking
Smoking
391 0 2 3.4E-03 0 0
CUI: C0013132
Disease: Drooling
Drooling
95 0 1 3.4E-03 0 0
CUI: C0023015
Disease: Language Disorders
Language Disorders
94 0 1 3.5E-03 0 0
CUI: C0270850
Disease: Idiopathic generalized epilepsy
Idiopathic generalized epilepsy
94 0 1 3.5E-03 0 0
CUI: C0850703
Disease: Frequent falls
Frequent falls
94 0 1 3.5E-03 0 0
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized
93 0 1 3.5E-03 0 0
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy
93 0 1 3.5E-03 0 0
CUI: C0431904
Disease: Ulnar polydactyly of fingers
Ulnar polydactyly of fingers
92 0 1 3.5E-03 0 0
CUI: C0426886
Disease: Tapering fingers (finding)
Tapering fingers (finding)
91 0 1 3.5E-03 0 0
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
90 0 1 3.5E-03 0 0
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele
89 0 1 3.5E-03 0 0
CUI: C1963060
Disease: Agitation, CTCAE 3.0
Agitation, CTCAE 3.0
87 0 1 3.5E-03 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness
87 0 1 3.5E-03 0 0
CUI: C4552855
Disease: Agitation, CTCAE 5.0
Agitation, CTCAE 5.0
87 0 1 3.5E-03 0 0
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome
86 0 1 3.6E-03 0 0