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: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 2.5E-03 0 0
CUI: C0265610
Disease: Clinodactyly of fingers
Clinodactyly of fingers
160 0 1 2.6E-03 0 0
CUI: C0038580
Disease: Substance Dependence
Substance Dependence
156 0 1 2.6E-03 0 0
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia
152 0 1 2.6E-03 0 0
CUI: C4551485
Disease: Clinodactyly
Clinodactyly
148 0 1 2.7E-03 0 0
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
145 0 1 2.7E-03 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion
145 0 1 2.7E-03 0 0
CUI: C1868571
Disease: Highly arched eyebrow
Highly arched eyebrow
141 0 1 2.7E-03 0 0
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition
140 0 1 2.7E-03 0 0
CUI: C1963094
Disease: Dry Skin, CTCAE
Dry Skin, CTCAE
137 0 1 2.7E-03 0 0
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment
136 0 1 2.7E-03 0 0
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal
130 0 1 2.8E-03 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria
129 0 1 2.8E-03 0 0
CUI: C0266544
Disease: Microcornea
Microcornea
129 0 1 2.8E-03 0 0
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria
127 0 1 2.8E-03 0 0
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision
127 0 1 2.8E-03 0 0
CUI: C0240543
Disease: Bulbous nose
Bulbous nose
123 0 1 2.8E-03 0 0
CUI: C0685409
Disease: Congenital Camptodactyly
Congenital Camptodactyly
123 0 1 2.8E-03 0 0
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth
122 0 1 2.8E-03 0 0
CUI: C0034194
Disease: Pyloric Stenosis
Pyloric Stenosis
121 0 1 2.9E-03 0 0
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly
120 0 1 2.9E-03 0 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity
113 0 1 2.9E-03 0 0
CUI: C0431447
Disease: Synophrys
Synophrys
111 0 1 2.9E-03 0 0
CUI: C1843108
Disease: Short palm
Short palm
110 0 1 2.9E-03 0 0
CUI: C0079541
Disease: Holoprosencephaly
Holoprosencephaly
109 0 1 3.0E-03 0 0